US5145980A - Oxime ethers, and fungicides containing same - Google Patents
Oxime ethers, and fungicides containing same Download PDFInfo
- Publication number
- US5145980A US5145980A US07/509,588 US50958890A US5145980A US 5145980 A US5145980 A US 5145980A US 50958890 A US50958890 A US 50958890A US 5145980 A US5145980 A US 5145980A
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- United States
- Prior art keywords
- sub
- methyl
- cyclo
- oil
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
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- -1 Oxime ethers Chemical class 0.000 title claims abstract description 25
- 239000000417 fungicide Substances 0.000 title abstract description 10
- 150000001875 compounds Chemical class 0.000 claims abstract description 40
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims description 39
- 238000000034 method Methods 0.000 claims description 20
- 241000233866 Fungi Species 0.000 claims description 6
- 230000000855 fungicidal effect Effects 0.000 claims description 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 2
- 239000002689 soil Substances 0.000 claims description 2
- 101100434171 Oryza sativa subsp. japonica ACR2.2 gene Proteins 0.000 claims 1
- 230000002538 fungal effect Effects 0.000 claims 1
- 125000003707 hexyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract description 13
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract description 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract description 4
- 125000003118 aryl group Chemical group 0.000 abstract description 3
- 229910052736 halogen Inorganic materials 0.000 abstract description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract description 3
- 150000002367 halogens Chemical class 0.000 abstract description 2
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 101150035983 str1 gene Proteins 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 321
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 33
- 239000003921 oil Substances 0.000 description 31
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 27
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 24
- 239000000243 solution Substances 0.000 description 20
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 12
- 239000004480 active ingredient Substances 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 11
- 239000012043 crude product Substances 0.000 description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 9
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 8
- 229910052938 sodium sulfate Inorganic materials 0.000 description 8
- 235000011152 sodium sulphate Nutrition 0.000 description 8
- 241000196324 Embryophyta Species 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 238000004817 gas chromatography Methods 0.000 description 6
- SHFJWMWCIHQNCP-UHFFFAOYSA-M hydron;tetrabutylazanium;sulfate Chemical compound OS([O-])(=O)=O.CCCC[N+](CCCC)(CCCC)CCCC SHFJWMWCIHQNCP-UHFFFAOYSA-M 0.000 description 6
- BTFQKIATRPGRBS-UHFFFAOYSA-N o-tolualdehyde Chemical compound CC1=CC=CC=C1C=O BTFQKIATRPGRBS-UHFFFAOYSA-N 0.000 description 6
- 239000012074 organic phase Substances 0.000 description 6
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 238000009472 formulation Methods 0.000 description 5
- QMJRGFDWGOXABE-UHFFFAOYSA-N methyl 2-(2-methylphenyl)-2-oxoacetate Chemical compound COC(=O)C(=O)C1=CC=CC=C1C QMJRGFDWGOXABE-UHFFFAOYSA-N 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000000741 silica gel Substances 0.000 description 5
- 229910002027 silica gel Inorganic materials 0.000 description 5
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- NPTHQXSIHOKQDP-UHFFFAOYSA-N 2-[(2,4-dimethylphenoxy)methyl]benzaldehyde Chemical compound CC1=CC(C)=CC=C1OCC1=CC=CC=C1C=O NPTHQXSIHOKQDP-UHFFFAOYSA-N 0.000 description 4
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000005708 Sodium hypochlorite Substances 0.000 description 4
- 229950005499 carbon tetrachloride Drugs 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 235000013339 cereals Nutrition 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 239000003701 inert diluent Substances 0.000 description 4
- 239000012442 inert solvent Substances 0.000 description 4
- YCINJZQUXAFTQD-UHFFFAOYSA-N methyl 2-methoxyimino-2-(2-methylphenyl)acetate Chemical compound CON=C(C(=O)OC)C1=CC=CC=C1C YCINJZQUXAFTQD-UHFFFAOYSA-N 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 150000002989 phenols Chemical class 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- QGXNHCXKWFNKCG-UHFFFAOYSA-N 2-(bromomethyl)benzonitrile Chemical compound BrCC1=CC=CC=C1C#N QGXNHCXKWFNKCG-UHFFFAOYSA-N 0.000 description 3
- 239000001431 2-methylbenzaldehyde Substances 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- 240000005979 Hordeum vulgare Species 0.000 description 3
- 235000007340 Hordeum vulgare Nutrition 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 3
- 241000209140 Triticum Species 0.000 description 3
- 235000021307 Triticum Nutrition 0.000 description 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
- AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- 239000004359 castor oil Substances 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
- LDPXOYHMGOQPIV-UHFFFAOYSA-N methyl 2-[2-(bromomethyl)phenyl]-2-methoxyiminoacetate Chemical compound CON=C(C(=O)OC)C1=CC=CC=C1CBr LDPXOYHMGOQPIV-UHFFFAOYSA-N 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- LGZDNJBUAAXEMN-UHFFFAOYSA-N 1,2,2,3-tetramethyl-1-oxidopiperidin-1-ium Chemical compound CC1CCC[N+](C)([O-])C1(C)C LGZDNJBUAAXEMN-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 2
- WYXWANVHOUGOBI-UHFFFAOYSA-N 2-methylbenzoyl cyanide Chemical compound CC1=CC=CC=C1C(=O)C#N WYXWANVHOUGOBI-UHFFFAOYSA-N 0.000 description 2
- YYYWRLBPLMADTB-UHFFFAOYSA-N 7-[bis(3,6-dioxoheptyl)amino]heptane-2,5-dione Chemical compound CC(=O)CCC(=O)CCN(CCC(=O)CCC(C)=O)CCC(=O)CCC(C)=O YYYWRLBPLMADTB-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- 229910003556 H2 SO4 Inorganic materials 0.000 description 2
- WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 244000070406 Malus silvestris Species 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 241000520648 Pyrenophora teres Species 0.000 description 2
- 240000000111 Saccharum officinarum Species 0.000 description 2
- 235000007201 Saccharum officinarum Nutrition 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 241000219094 Vitaceae Species 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- 235000021016 apples Nutrition 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 150000008359 benzonitriles Chemical class 0.000 description 2
- SIPUZPBQZHNSDW-UHFFFAOYSA-N bis(2-methylpropyl)aluminum Chemical compound CC(C)C[Al]CC(C)C SIPUZPBQZHNSDW-UHFFFAOYSA-N 0.000 description 2
- 159000000007 calcium salts Chemical class 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 2
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- GUVUOGQBMYCBQP-UHFFFAOYSA-N dmpu Chemical compound CN1CCCN(C)C1=O GUVUOGQBMYCBQP-UHFFFAOYSA-N 0.000 description 2
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 235000021021 grapes Nutrition 0.000 description 2
- XNXVOSBNFZWHBV-UHFFFAOYSA-N hydron;o-methylhydroxylamine;chloride Chemical compound Cl.CON XNXVOSBNFZWHBV-UHFFFAOYSA-N 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- BLEMRRXGTKTJGT-UHFFFAOYSA-N methyl 2-(2-methylphenyl)acetate Chemical compound COC(=O)CC1=CC=CC=C1C BLEMRRXGTKTJGT-UHFFFAOYSA-N 0.000 description 2
- ZNQKFRXUOKNZGV-UHFFFAOYSA-N methyl 2-[2-[(2,4-dimethylphenoxy)methyl]phenyl]-2-hydroxyacetate Chemical compound COC(=O)C(O)C1=CC=CC=C1COC1=CC=C(C)C=C1C ZNQKFRXUOKNZGV-UHFFFAOYSA-N 0.000 description 2
- RMUPWIFDZMWSJQ-UHFFFAOYSA-N methyl 2-hydroxy-2-(2-methylphenyl)acetate Chemical compound COC(=O)C(O)C1=CC=CC=C1C RMUPWIFDZMWSJQ-UHFFFAOYSA-N 0.000 description 2
- YTLSSHQATHKKNF-UHFFFAOYSA-N methyl 2-methoxyimino-2-[2-(phenoxymethyl)phenyl]acetate Chemical compound CON=C(C(=O)OC)C1=CC=CC=C1COC1=CC=CC=C1 YTLSSHQATHKKNF-UHFFFAOYSA-N 0.000 description 2
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 2
- 239000012022 methylating agents Substances 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 150000002923 oximes Chemical class 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 239000003444 phase transfer catalyst Substances 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- ZGJADVGJIVEEGF-UHFFFAOYSA-M potassium;phenoxide Chemical class [K+].[O-]C1=CC=CC=C1 ZGJADVGJIVEEGF-UHFFFAOYSA-M 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- JZHCCZPNFQSNBE-UHFFFAOYSA-M sodium;2,4-dimethylphenolate Chemical compound [Na+].CC1=CC=C([O-])C(C)=C1 JZHCCZPNFQSNBE-UHFFFAOYSA-M 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- IOGXOCVLYRDXLW-UHFFFAOYSA-N tert-butyl nitrite Chemical compound CC(C)(C)ON=O IOGXOCVLYRDXLW-UHFFFAOYSA-N 0.000 description 2
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 2
- WFEXFNMTEBFLMM-UHFFFAOYSA-M trioctyl(propyl)azanium;chloride Chemical compound [Cl-].CCCCCCCC[N+](CCC)(CCCCCCCC)CCCCCCCC WFEXFNMTEBFLMM-UHFFFAOYSA-M 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- FIARMZDBEGVMLV-UHFFFAOYSA-N 1,1,2,2,2-pentafluoroethanolate Chemical group [O-]C(F)(F)C(F)(F)F FIARMZDBEGVMLV-UHFFFAOYSA-N 0.000 description 1
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 1
- 125000006017 1-propenyl group Chemical group 0.000 description 1
- KBLAMUYRMZPYLS-UHFFFAOYSA-N 2,3-bis(2-methylpropyl)naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(O)(=O)=O)=C(CC(C)C)C(CC(C)C)=CC2=C1 KBLAMUYRMZPYLS-UHFFFAOYSA-N 0.000 description 1
- XVCKAKIDFPGXBI-UHFFFAOYSA-N 2-[(2,4-dimethylphenoxy)methyl]benzonitrile Chemical compound CC1=CC(C)=CC=C1OCC1=CC=CC=C1C#N XVCKAKIDFPGXBI-UHFFFAOYSA-N 0.000 description 1
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 1
- UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 1
- FCSKOFQQCWLGMV-UHFFFAOYSA-N 5-{5-[2-chloro-4-(4,5-dihydro-1,3-oxazol-2-yl)phenoxy]pentyl}-3-methylisoxazole Chemical compound O1N=C(C)C=C1CCCCCOC1=CC=C(C=2OCCN=2)C=C1Cl FCSKOFQQCWLGMV-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 241000223600 Alternaria Species 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
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- 241000235349 Ascomycota Species 0.000 description 1
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- 244000075850 Avena orientalis Species 0.000 description 1
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- 241001480061 Blumeria graminis Species 0.000 description 1
- 241000123650 Botrytis cinerea Species 0.000 description 1
- 241000079253 Byssochlamys spectabilis Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 240000007154 Coffea arabica Species 0.000 description 1
- 240000008067 Cucumis sativus Species 0.000 description 1
- 235000009849 Cucumis sativus Nutrition 0.000 description 1
- 241000371644 Curvularia ravenelii Species 0.000 description 1
- 241000510928 Erysiphe necator Species 0.000 description 1
- QQZWEECEMNQSTG-UHFFFAOYSA-N Ethyl nitrite Chemical compound CCON=O QQZWEECEMNQSTG-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 240000009088 Fragaria x ananassa Species 0.000 description 1
- 241000223218 Fusarium Species 0.000 description 1
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- 241000896246 Golovinomyces cichoracearum Species 0.000 description 1
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- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 241001330975 Magnaporthe oryzae Species 0.000 description 1
- 229910021204 NaH2 PO4 Inorganic materials 0.000 description 1
- 229910019093 NaOCl Inorganic materials 0.000 description 1
- 241001668536 Oculimacula yallundae Species 0.000 description 1
- 101100434170 Oryza sativa subsp. japonica ACR2.1 gene Proteins 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 241000736122 Parastagonospora nodorum Species 0.000 description 1
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- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
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- 235000007238 Secale cereale Nutrition 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
- 241000221566 Ustilago Species 0.000 description 1
- 241000228452 Venturia inaequalis Species 0.000 description 1
- 241000082085 Verticillium <Phyllachorales> Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- GHVZOJONCUEWAV-UHFFFAOYSA-N [K].CCO Chemical compound [K].CCO GHVZOJONCUEWAV-UHFFFAOYSA-N 0.000 description 1
- JFBZPFYRPYOZCQ-UHFFFAOYSA-N [Li].[Al] Chemical compound [Li].[Al] JFBZPFYRPYOZCQ-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 230000002152 alkylating effect Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 150000003935 benzaldehydes Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 235000016213 coffee Nutrition 0.000 description 1
- 235000013353 coffee beverage Nutrition 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 description 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- XPYGGHVSFMUHLH-UUSULHAXSA-N falecalcitriol Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@@H](CCCC(O)(C(F)(F)F)C(F)(F)F)C)=C\C=C1\C[C@@H](O)C[C@H](O)C1=C XPYGGHVSFMUHLH-UUSULHAXSA-N 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- HHLFWLYXYJOTON-UHFFFAOYSA-N glyoxylic acid Chemical compound OC(=O)C=O HHLFWLYXYJOTON-UHFFFAOYSA-N 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 125000006277 halobenzyl group Chemical group 0.000 description 1
- 125000005059 halophenyl group Chemical group 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000003898 horticulture Methods 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- YOBAEOGBNPPUQV-UHFFFAOYSA-N iron;trihydrate Chemical compound O.O.O.[Fe].[Fe] YOBAEOGBNPPUQV-UHFFFAOYSA-N 0.000 description 1
- OWFXIOWLTKNBAP-UHFFFAOYSA-N isoamyl nitrite Chemical compound CC(C)CCON=O OWFXIOWLTKNBAP-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 229910052987 metal hydride Inorganic materials 0.000 description 1
- 150000004681 metal hydrides Chemical class 0.000 description 1
- IWVCHTDPZIEDCQ-UHFFFAOYSA-N methyl 2-[2-[(2,4-dimethylphenoxy)methyl]phenyl]-2-methoxyiminoacetate Chemical compound CON=C(C(=O)OC)C1=CC=CC=C1COC1=CC=C(C)C=C1C IWVCHTDPZIEDCQ-UHFFFAOYSA-N 0.000 description 1
- DLIQQCPRDSZBEF-UHFFFAOYSA-N methyl 2-[2-[(2,4-dimethylphenoxy)methyl]phenyl]-2-oxoacetate Chemical compound COC(=O)C(=O)C1=CC=CC=C1COC1=CC=C(C)C=C1C DLIQQCPRDSZBEF-UHFFFAOYSA-N 0.000 description 1
- BXLJNVXXPYDYBS-UHFFFAOYSA-N methyl 2-hydroxyimino-2-(2-methylphenyl)acetate Chemical compound COC(=O)C(=NO)C1=CC=CC=C1C BXLJNVXXPYDYBS-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- SQDFHQJTAWCFIB-UHFFFAOYSA-N n-methylidenehydroxylamine Chemical class ON=C SQDFHQJTAWCFIB-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- 235000021012 strawberries Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- AXZWODMDQAVCJE-UHFFFAOYSA-L tin(II) chloride (anhydrous) Chemical compound [Cl-].[Cl-].[Sn+2] AXZWODMDQAVCJE-UHFFFAOYSA-L 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 238000009369 viticulture Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C255/54—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and etherified hydroxy groups bound to the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/32—Oximes
- C07C251/62—Oximes having oxygen atoms of oxyimino groups esterified
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/50—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids the nitrogen atom being doubly bound to the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/27—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups
- C07C205/35—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C205/36—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system
- C07C205/37—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/32—Oximes
- C07C251/34—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
- C07C251/48—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with the carbon atom of at least one of the oxyimino groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/32—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring
- C07C255/37—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by etherified hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/44—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reduction and hydrolysis of nitriles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/52—Compounds having —CHO groups bound to carbon atoms of six—membered aromatic rings
- C07C47/575—Compounds having —CHO groups bound to carbon atoms of six—membered aromatic rings containing ether groups, groups, groups, or groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/734—Ethers
- C07C69/736—Ethers the hydroxy group of the ester being etherified with a hydroxy compound having the hydroxy group bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/738—Esters of keto-carboxylic acids or aldehydo-carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/10—One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline
Definitions
- the present invention relates to novel oxime ethers, their preparation, fungicides containing same, and their use as fungicides.
- oxime ether derivatives such as, for example, methyl 2-phenoxymethylphenylglyoxylate O-methyl oxime, as fungicides (EP 253,213 and EP 254,426).
- novel compounds of the general formula I can exist in the form of either E or Z isomers, which can be separated in the customary manner.
- the individual isomeric compounds and their mixtures are covered by the invention and can be used as fungicides.
- the known methyl 2-methylphenylglyoxylate VI (cf., for example, J.M. Photis, Tetrahedron Lett. 1980, 3539) can be prepared, for example, by converting 2-methylbenzaldehyde by known processes using potassium cyanide or sodium cyanide into 2-methylbenzaldehydecyanohydrin, from which methyl 2-methylmandelate can be prepared in the presence of methanol and a protic acid, such as, for example, hydrochloric acid (cf., for example, U.S. Pat. No. 2,892,847).
- a protic acid such as, for example, hydrochloric acid
- Methyl 2-methylphenylglyoxylate O-methyl oxime VII can be prepared by reacting methyl 2-methylphenylglyoxylate VI, for example, a) with O-methylhydroxylamine hydrochloride or b) with hydroxylamine hydrochloride to give the corresponding oxime, and reacting the latter with a methylating agent of the formula CH 3 -L, in which L is a leaving group (for example chloride, bromide, iodide or methylsulfate) (cf. EP 253,213).
- a methylating agent of the formula CH 3 -L, in which L is a leaving group (for example chloride, bromide, iodide or methylsulfate)
- Methyl 2-methylphenylglyoxylate O-methyl oxime VII can also be prepared by oximating methyl 2-methylphenylacetate in a manner known per se (cf., for example, Houben-Weyl, Methoden der organischen Chemie [Methods of Organic Chemistry], Volume 10/4, pp.
- alkyl nitrite such as, for example, ethyl nitrite, tert.-butyl nitrite or isoamyl nitrite
- a suitable base such as, for example, sodium ethylate, potassium ethylate or potassium tert.-butylate, and alkylating the methyl 2-methylphenylglyoxylate oxime obtained in this way as described above.
- the benzyl bromide VIII can be prepared by known methods by reacting the compound VII for example with bromine in a solvent, such as, for example, tetrachloromethane, if necessary with irradiation using a light source (for example Hg vapor lamp, 300 W) or with N-bromosuccinimide (Horner, Winkelmann, Angew. Chem. 71, 349 (1959)).
- a solvent such as, for example, tetrachloromethane
- novel compounds of the general formula I according to claim 1 are prepared, for example, by reacting an appropriately substituted phenol with the benzyl bromide VIII.
- the reactions can be carried out, for example, in an inert solvent or diluent (for example acetone, acetonitrile, dimethyl sulfoxide, dimethylformamide, N-methylpyrrolidone, N,N'-dimethylpropyleneurea or pyridine) using a base (for example sodium carbonate or potassium carbonate).
- a base for example sodium carbonate or potassium carbonate.
- a catalyst such as, for example, tris-(3,6-dioxoheptyl)amine, to the reaction mixture.
- a procedure may also be adopted in which the phenols are first converted using a base (for example sodium hydroxide, potassium hydroxide or sodium methanolate) into the corresponding sodium or potassium phenolates and the latter are then reacted with the benzyl bromide VIII in an inert solvent or diluent (for example dimethylformamide) to form the compounds of the general formula I.
- a base for example sodium hydroxide, potassium hydroxide or sodium methanolate
- an inert solvent or diluent for example dimethylformamide
- phase-transfer catalysts are, for example, trioctylpropylammonium chloride or cetyltrimethylammonium chloride.
- the reactions may be carried out, for example, in an inert solvent or diluent (for example acetone, dimethyl sulfoxide, dimethylformamide, N-methylpyrrolidone, N,N'-dimethylpropyleneurea or pyridine) using a base (for example sodium carbonate or potassium carbonate).
- a base for example sodium carbonate or potassium carbonate.
- a catalyst such as, for example, tris-(3,6-dioxoheptyl)amine, to the reaction mixture.
- a procedure may be adopted in which the phenols are first converted using a base (for example sodium hydroxide, potassium hydroxide or sodium methanolate) into the corresponding sodium or potassium phenolates, and the latter are then reacted with 2-(bromomethyl)benzonitrile in an inert solvent or diluent (for example dimethylformamide).
- a base for example sodium hydroxide, potassium hydroxide or sodium methanolate
- 2-(bromomethyl)benzonitrile in an inert solvent or diluent (for example dimethylformamide).
- phase-transfer catalysts are, for example, trioctylpropylammonium chloride or cetyltrimethylammonium chloride.
- Benzonitriles of the general formula IX are reduced to the benzaldehyde derivatives of the general formula V.
- the reduction is carried out, for example, using hydrochloric acid/tin(II) chloride (Stephen reduction, cf., for example, Zil'berman, Pyryalova, J. Gen. Chem. USSR 33, (1964) 3348) or using a metal hydride, such as, for example, lithium aluminum or diisobutylaluminum hydride (cf., for example, Marshall, Andersen, Scheuer, J. Org. Chem. 35, (1970) 858).
- a metal hydride such as, for example, lithium aluminum or diisobutylaluminum hydride
- Benzaldehyde cyanohydrins of the general formula IV can be prepared from the aldehydes of the general formula V in a generally known manner, for example using potassium cyanide or sodium cyanide.
- the compounds of the general formula IV are novel and are likewise covered by this invention.
- methanol and a protic acid such as, for example, hydrochloric acid, they can be converted into the mandelates of the general formula III (cf., for example, U.S. Pat. No. 2,892,847).
- the compounds of the general formula III are novel and are likewise covered by this invention. Reaction of them with a suitable oxidant, such as, for example, sodium hypochlorite, if necessary in the presence of an appropriate catalyst, such as tetrabutylammonium bisulfate, tetrabutylammonium bromide (cf., for example, EP 140,454) or tetramethylpiperidine N-oxide, gives methyl alpha-ketocarboxylates of the general formula II.
- a suitable oxidant such as, for example, sodium hypochlorite
- an appropriate catalyst such as tetrabutylammonium bisulfate, tetrabutylammonium bromide (cf., for example, EP 140,454) or tetramethylpiperidine N-oxide
- the compounds of the general formula II are novel and are likewise covered by this invention. From them, the compounds of the general structure I according to the invention can be synthesized in a known manner (cf. EP 253,213) by reaction, for example, a) with O-methylhydroxylamine hydrochloride or b) with hydroxylamine to form the corresponding oxime and reaction of the latter with a methylating agent of the formula CH 3 -L, in which L is a leaving group (for example chloride, bromide or methylsulfate).
- 275 g of the crude product from method 1 are dissolved in 750 ml of methanol, and the solution is added to 7.5 molar methanolic hydrochloric acid (620 ml). The mixture is stirred at room temperature for 15 hours. The pH is subsequently adjusted to 3 using NaOH/H 2 O, and the mixture is stirred for a further 2 hours. The product is extracted using methylene chloride, and the extracts are dried and evaporated. 280.5 g of crude product (content of end product according to gas chromatography (GC) 76%) yield: 76%.
- GC gas chromatography
- the potassium salt slowly dissolves, and microcrystalline potassium iodide precipitates.
- the mixture is stirred at room temperature overnight and evaporated, the residue is taken up in methyl tert.-butyl ether/H 2 O, and the solution is washed several times with H 2 O, dried over sodium sulfate and re-evaporated.
- Methyl 2-(bromomethyl)phenylglyoxylate O-methyl oxime (VIII) 21.4 g (0.133 mol) of bromine are added with stirring to 27.5 g (0.133 mol) of methyl 2-methylphenylglyoxylate O-methyl oxime dissolved in 400 ml of tetrachloromethane. The mixture is then heated at the reflux temperature for four hours while being irradiated with a 300 W Hg vapor lamp. The mixture is then evaporated, the residue is taken up in ethyl acetate/water, and the solution is washed with H 2 O, dried using sodium sulfate and evaporated. The crude product is purified by chromatography on silica gel using cyclohexane/ethyl acetate (9/1). 17.4 g (46%) of the abovementioned compound are obtained as an oil.
- novel compounds are extremely effective on a broad spectrum of phytopathogenic fungi, in particular those from the Ascomycetes and Basidiomycetes classes. Some of them have a systemic action and can be sued as foliar and soil fungicides.
- the fungicidal compounds are of particular interest for controlling a large number of fungi in various crops or their seeds, especially wheat, rye, barley, oats, rice, Indian corn, lawns, cotton, soybeans, coffee, sugar cane, fruit and ornamentals in horticulture and viticulture, and in vegetables such as cucumbers, beans and cucurbits.
- novel compounds are particularly useful for controlling the following plant diseases:
- Botrytis cinerea (gray mold) in strawberries and grapes
- the compounds are applied by spraying or dusting the plants with the active ingredients, or treating the seeds of the plants with the active ingredients. They may be applied before or after infection of the plants or seeds by the fungi.
- novel substances can be converted into conventional formulations such as solutions, emulsions, suspensions, dusts, powders, pastes and granules.
- the application forms depend entirely on the purposes for which they are intended; they should at all events ensure a fine and uniform distribution of the active ingredient.
- the formulations are produced in known manner, for example by extending the active ingredient with solvent and/or carriers, with or without the use of emulsifiers and dispersants; if water is used as solvent, it is also possible to employ other organic solvents as auxiliary solvent.
- auxiliaries for this purpose are solvents such as aromatics (e.g., xylene), chlorinated aromatics (e.g., chlorobenzenes), paraffins (e.g., crude oil fractions), alcohols (e.g., methanol, butanol), ketones (e.g., cyclohexanone), amines (e.g., ethanolamine, dimethylformamide), and water; carriers such as ground natural minerals (e.g., kaolins, aluminas, talc and chalk) and ground synthetic minerals (e.g., highly disperse silica and silicates); emulsifiers such as nonionic and anionic emulsifiers (e.g., polyoxyethylene fatty alcohol ethers, alkyl sulfonates and aryl sulfonates); and dispersants such as lignin, sulfite waste liquors and methylcellulose.
- solvents such as aromatics (e.g.,
- the fungicidal agents generally contain from 0.1 to 95, and preferably from 0.5 to 90, wt% of active ingredient
- the application rates are from 0.02 to 3 kg or more of active ingredient per hectare, depending on the type of effect desired.
- the novel compounds may also be used for protecting materials, for example against Paecilomyces variotii.
- the active ingredients When the active ingredients are used for treating seed, amounts of from 0.001 to 50, and preferably from 0.01 to 10, g per kg of seed are usually employed.
- agents and the ready-to-use formulations prepared from them are applied in conventional manner, for example by spraying, atomizing, dusting, scattering, dressing or watering.
- V. 80 parts by weight of compound no. 1.10 is well mixed with 3 parts by weight of the sodium salt of diisobutylnaphthalene- ⁇ -sulfonic acid, 10 parts by weight of the sodium salt of a lignin-sulfonic acid obtained from a sulfite waste liquor, and 7 parts by weight of powdered silica gel, and triturated in a hammer mill. By uniformly distributing the mixture in water, a spray liquor is obtained.
- the agents according to the invention may also be present together with other active ingredients, for example herbicides, insecticides, growth regulators, and fungicides, and may furthermore be mixed and applied together with fertilizers. Admixture with other fungicides frequently results in an increase in the fungicidal spectrum.
- Barley seedings of the "Igri" variety were sprayed to runoff at the two-leaf stage with aqueous suspensions consisting (dry basis) of 80% of active ingredient and 20% of emulsifier. After 24 hours the plants were inoculated with a spore suspension of the fungus Pyrenophora teres, and set up for 48 hours in a high-humidity climatic cabinet at 18° C. The plants were then cultivated for a further 5 days in the greenhouse at 20° to 22° C. and a relative humidity of 70° C. The extent of fungus spread was then assessed.
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Abstract
Description
TABLE 1
__________________________________________________________________________
##STR5## I
No. X.sub.m mp (°C.)
IR(cm.sup.-1)
__________________________________________________________________________
1. 1
3-F 72-75
2945, 1728, 1593, 1490, 1220, 1135, 1070, 1020
1. 2
4-F 74-76
2970, 1733, 1726, 1508, 1222, 1204, 1070, 1016
1. 3
2,4-F.sub.2 75-76
2960, 1738, 1515, 1267, 1212, 1068, 1007, 768
1. 4
2,4,6-F.sub.3
1. 5
2,3,4,5,6-F.sub.5
1. 6
2,3-F.sub.2
1. 7
2,3-Cl.sub.2 105-108
2955, 1743, 1456, 1303, 1068, 1015, 769
1. 8
2,5-Cl.sub.2 145-147
2945, 1738, 1583, 1379, 1301, 1248, 1069, 1009
1. 9
2,6-Cl.sub.2 115-118
2945, 1729, 1444, 1250, 1061, 1009, 772
1. 10
3,4-Cl.sub.2 90-92
2950, 1740, 1591, 1468, 1300, 1225, 1070, 1013
1. 11
3,5-Cl.sub.2 115-117
3080, 2945, 1743, 1587, 1573, 1306, 1070, 1008
1. 12
2,3,4-Cl.sub.3
1. 13
2,3,5-Cl.sub.3
1. 14
2,3,6-Cl.sub.3
1. 15
2,4,5-Cl.sub.3
1. 16
2,4,6-Cl.sub.3
1. 17
3,4,5-Cl.sub.3
1. 18
2,3,4,6-Cl.sub.4
1. 19
2,3,5,6-Cl.sub.4
1. 20
2,3,4,5,6-Cl.sub.5
1. 21
2-Br 94-97
2950, 1729, 1479, 1241, 1065, 1018, 746
1. 22
3-Br 66-67
2945, 1738, 1595, 1307, 1245, 1228, 1069, 1010
1. 23
4-Br 94-96
2945, 1739, 1486, 1286, 1231, 1067, 1008, 824
1. 24
2,4-Br.sub.2 106-108
2950, 1727, 1474, 1278, 1224, 1066, 1014
1. 25
2,5-Br.sub.2
1. 26
2,6-Br.sub.2
1. 27
2,4,6-Br.sub.3
1. 28
2,3,4,5,6-Br.sub.5
1. 29
2-I 80-83
2950, 1715, 1442, 1222, 1069, 1012, 744
1. 30
3-I
1. 31
4-I
1. 32
2,4-I.sub.2
1. 33
2-Cl, 3-F
1. 34
2-Cl, 4-F 73-75
2950, 1741, 1503, 1302, 1197, 1069, 1009, 791
1. 35
2-Cl, 5-F
1. 36
2-Cl, 6-F
1. 37
2-Cl, 3-Br
1. 38
2-Cl, 4-Br 114-116
2945, 1728, 1479, 1435, 1264, 1243, 1067, 1015
1. 39
2-Cl, 5-Br
1. 40
2-Cl, 6-Br
1. 41
2-Br, 3-Cl
1. 42
2-Br, 4-Cl 117-120
2940, 1723, 1479, 1441, 1218, 1067, 1021, 791
1. 43
2-Br, 3-F
1. 45
2-Br, 4-F 81-84
2960, 1725, 1498, 1434, 1265, 1197, 1068, 1013
1. 46
2-Br, 5-F
1. 47
2-Br, 6-F
1. 48
2-F, 3-Cl
1. 49
2-F, 4-Cl
1. 50
2-F, 5-Cl
1. 51
3-Cl, 4-F 86-89
2945, 1725, 1499, 1227, 1213, 1069, 1011, 785
1. 52
3-Cl, 5-F
1. 53
3-Cl, 4-Br
1. 54
3-Cl, 5-Br
1. 55
3-F, 4-Cl
1. 56
3-F, 4-Br
1. 57
3-Br, 4-Cl
1. 58
3-Br, 4-F
1. 59
2,6-Cl.sub.2, 4-Br
1. 60
3-CH.sub.3 72 2950, 1729, 1256, 1152, 1066, 1010, 779
1. 61
2,3-(CH.sub.3).sub.2
110-113
2945, 1740, 1467, 1302, 1256, 1062, 1013, 771
1. 62
2,4-(CH.sub.3).sub.2
68-74
2945, 1739, 1504, 1253, 1223, 1065, 1005, 769
1. 63
2,5-(CH.sub.3).sub.2
103-105
1. 64
2,6-(CH.sub.3).sub.2
85-88
1741, 1438, 1297, 1230, 1196, 1068, 1012, 997,
773
1. 65
3,4-(CH.sub.3).sub.2
89-93
1724, 1502, 1251, 1225, 1203, 1163, 1067, 1030,
1012, 954
1. 66
3,5-(CH.sub.3).sub.2
80-83
1739, 1594, 1322, 1302, 1222, 1152, 1078, 1065,
1009, 825
1. 67
2,3,4-(CH.sub.3).sub.3
1. 68
2,3,5-(CH.sub.3).sub.3
97-98
2940, 1740, 1300, 1219, 1067, 1008, 774
1. 69
2,3,6-(CH.sub.3).sub.3
1. 70
2,4,5-(CH.sub.3).sub.3
94-95
1. 71
2,4,6-(CH.sub.3).sub.3
113-115
1. 72
3,4,5-(CH.sub.3).sub.3
94-97
2960, 1719, 1441, 1317, 1223, 1145, 1065, 1020
1. 73
2,3,4,6-(CH.sub.3).sub.4
1. 74
2,3,5,6-(CH.sub.3).sub.4
1. 75
2,3,4,5,6-(CH.sub.3).sub.5
1. 76
2-C.sub.2 H.sub.5
46-48
2960, 1739, 1493, 1435, 1222, 1067, 748
1. 77
3-C.sub.2 H.sub.5
1. 78
4-C.sub.2 H.sub.5
1. 79
2,4-(C.sub.2 H.sub.5).sub.2
1. 80
2,6-(C.sub.2 H.sub.5).sub.2
1. 81
3,5-(C.sub.2 H.sub.5).sub.2
oil 2963, 1727, 1592, 1455, 1339, 1285, 1218, 1152,
1069, 1020
1. 82
2,4,6-(C.sub.2 H.sub.5).sub.3
1. 83
2-n-C.sub.3 H.sub.7
44-46
2955, 1727, 1492, 1321, 1221, 1069, 1019, 752
1. 84
3-n-C.sub.3 H.sub.7
1. 85
4-n-C.sub.3 H.sub.7
1. 86
2-i-C.sub.3 H.sub.7
oil 2950, 1727, 1491, 1233, 1223, 1069, 1019, 753
1. 87
3-i-C.sub.3 H.sub.7
1. 88
4-i-C.sub.3 H.sub.7
oil 2958, 1728, 1512, 1222, 1070, 1019
1. 89
2,4-(i-C.sub.3 H.sub.7).sub.2
oil 2956, 1728, 1498, 1216, 1069, 1020
1. 90
2,6-(i-C.sub.3 H.sub.7).sub.2
1. 91
3,5-(i-C.sub.3 H.sub.7).sub.2
oil 2960, 1728, 1594, 1447, 1219, 1069, 1021
1. 92
2,4,6-(i-C.sub.3 H.sub.7).sub.3
1. 93
2-s-C.sub.4 H.sub.9
oil 2960, 1727, 1490, 1448, 1438, 1221, 1069, 1047,
1019, 752
1. 94
3-s-C.sub.4 H.sub.9
1. 95
4-s-C.sub.4 H.sub.9
1. 96
2-t-C.sub.4 H.sub.9
1. 97
3-t-C.sub.4 H.sub.9
oil 2962, 1728, 1582, 1437, 1274, 1219, 1069, 1020
1. 98
2,3-(t-C.sub.4 H.sub.9).sub.2
1. 99
2,4-(t-C.sub.4 H.sub.9).sub.2
1. 100
2,5-(t-C.sub.4 H.sub.9).sub.2
1. 101
2,6-(t-C.sub.4 H.sub.9).sub.2
1. 102
3,5-(t-C.sub.4 H.sub.9).sub.2
oil 2963, 1729, 1592, 1302, 1219, 1070, 1020
1. 103
2,4,6-(t-C.sub.4 H.sub.9).sub.3
1. 104
4-n-C.sub.9 H.sub.19
oil 2956, 2935, 2871, 1727, 1510, 1244, 1220, 1183,
1069, 1019
1. 105
4-n-C.sub.12 H.sub.25
1. 106
3-n-C.sub.15 H.sub.31
1. 107
4-(1,1,3,3-tetramethylbutyl)
oil 2954, 1728, 1511, 1317, 1303, 1245, 1220, 1183,
1069, 1020
1. 108
4-(2,3,3-tri-methylpropyl)
1. 109
2-t-C.sub.4 H.sub.9, 4-CH.sub.3
1. 110
2-t-C.sub.4 H.sub.9, 5-CH.sub.3
1. 111
2,6-(t-C.sub.4 H.sub.9).sub.2, 4-CH.sub. 3
1. 112
2-CH.sub.3, 4-t-C.sub.4 H.sub.9
1. 113
2-CH.sub.3, 6-t-C.sub.4 H.sub.9
1. 114
2-CH.sub.3, 4-i-C.sub.3 H.sub.7
1. 115
2-CH.sub.3, 5-i-C.sub.3 H.sub.7
oil 2957, 1727, 1437, 1252, 1218, 1069, 1020
1. 116
3-CH.sub.3, 4-i-C.sub.3 H.sub.7
1. 117
2-i-C.sub.3 H.sub.7, 5-CH.sub.3
70-74
2958, 1727, 1505, 1437, 1290, 1255, 1219, 1069,
1045, 1020
1. 118
2,4-(t-C.sub.4 H.sub.9).sub.2, 6-i-C.sub.3 H.sub.7
1. 119
2-C.sub.3 H.sub.5 (= allyl)
47 2945, 1739, 1493, 1304, 1251, 1069, 1010, 744
1. 120
3-C.sub.3 H.sub.5
1. 121
4-C.sub.3 H.sub.5
1. 122
2-C.sub.3 H.sub.5, 6-CH.sub.3
1. 123
2-cyclo-C.sub.6 H.sub.11
115 2924, 1726, 1239, 1228, 1068, 1016, 750
1. 124
3-cyclo-C.sub.6 H.sub.11
1. 125
4-cyclo-C.sub.6 H.sub.11
93 2923, 1731, 1510, 1239, 1232, 1063, 1020, 822
1. 126
2,4-(cyclo-C.sub.6 H.sub.11).sub.2, 6-CH.sub.3
1. 127
2-CH.sub.3, 4-cyclo-C.sub.6 H.sub.11
oil 2925, 2851, 1727, 1504, 1218, 1070, 1020
1. 128
2-CH.sub.2 C.sub.6 H.sub.5
1. 129
3-CH.sub.2 C.sub.6 H.sub.5
1. 130
4-CH.sub.2 C.sub.6 H.sub.5
1. 131
2-CH.sub.2 C.sub.6 H.sub.5, 4-CH.sub.3
oil 1726, 1501, 1495, 1452, 1249, 1220, 1069, 1019,
731
1. 132
2-CH.sub.3, 4-CH.sub.2 C.sub.6 H.sub.5
1. 133
2-C.sub.6 H.sub.5
oil 1739, 1725, 1481, 1434, 1263, 1220, 1069, 1017,
754, 699
1. 134
3-C.sub.6 H.sub.5
oil 1726, 1477, 1320, 1300, 1219, 1202, 1069, 1017,
759, 698
1. 135
4-C.sub.6 H.sub.5
resin
2955, 1729, 1519, 1488, 1245, 1069, 1015, 765
1. 136
4-(2-i-C.sub.3 H.sub.7C.sub.6 H.sub.4)
1. 137
4-C.sub.6 H.sub.5, 2,6-(CH.sub.3).sub.2
138-142
1739, 1474, 1305, 1295, 1229, 11789, 1068,
1010, 1001, 768
1. 138
2-Cl, 4-C.sub.6 H.sub.5
oil 2945, 1726, 1596, 1477, 1301, 1202, 1069, 759
1. 139
2-Br, 4-C.sub.6 H.sub.5
1. 140
2-C.sub.6 H.sub.5, 4-Cl
1. 141
2-C.sub.6 H.sub.5, 4-Br
1. 142
2-CH.sub.2 C.sub.6 H.sub.5, 4-Cl
1. 143
2-CH.sub.2 C.sub.6 H.sub.5, 4-Br
1. 144
2-Cl, 4-CH.sub.2 C.sub.6 H.sub.5
1. 145
2-Br, 4-CH.sub.2 C.sub.6 H.sub.5
1. 146
2-cyclo-C.sub.6 H.sub.11, 4-Cl
1. 147
2-cyclo-C.sub.6 H.sub.11, 4-Br
1. 148
2-Cl, 4-cyclo-C.sub.6 H.sub.11
1. 149
2-Br, 4-cyclo-C.sub.6 H.sub.11
1. 150
3-OCH.sub.3 69-71
2945, 1719, 1589, 1200, 1153, 1069, 1012, 756
1. 151
2,4-(OCH.sub.3).sub.2
1. 152
2-CF.sub.3
1. 153
3-CF.sub.3 46-48
2955, 1727, 1719, 1338, 1323, 1102, 1067, 1014
1. 154
4-CF.sub.3
1. 155
2-OCF.sub.3
1. 156
3-OCF.sub.3
1. 157
4-OCF.sub.3 resin
2950, 1731, 1506, 1242, 1222, 1119, 1069, 1017
1. 158
3-OCH.sub.2 CHF.sub.2
1. 159
2-NO.sub.2
1. 160
3-NO.sub.2 resin
1. 161
2-CN 103-105
2945, 2230, 1728, 1450, 1254, 1062, 1010, 762
1. 162
3-CN
1. 163
4-CN
1. 164
2-CH.sub.3, 3-Cl
1. 165
2-CH.sub.3, 5-Cl
1. 166
2-CH.sub.3, 6-Cl
1. 167
2-CH.sub.3, 3-F
1. 168
2-CH.sub.3, 4-F
1. 169
2-CH.sub.3, 5-F
1. 170
2-CH.sub.3, 6-F
1. 171
2-CH.sub.3, 3-Br
1. 172
2-CH.sub.3, 4-Br
1. 173
2-CH.sub.3, 5-Br
1. 174
2-CH.sub.3, 6-Br
1. 175
2-Cl, 3-CH.sub.3
1. 176
2-Cl, 4-CH.sub.3 90-92
1726, 1500, 1437, 1298, 1285, 1251, 1218, 1068,
1017
1. 177
2-Cl, 5-CH.sub.3 120-122
2940, 1737, 1489, 1309, 1070, 1065, 1008, 810
1. 178
2-F, 3-CH.sub.3
1. 179
2-F, 4-CH.sub.3
1. 180
2-F, 5-CH.sub.3
1. 181
2-Br, 3-CH.sub.3
1. 182
2-Br, 4-CH.sub.3
1. 183
3-CH.sub.3, 4-Cl
1. 184
3-CH.sub.3, 5-Cl
1. 185
2-Br, 5-CH.sub.3
1. 186
3-CH.sub.3, 4-F
1. 187
3-CH.sub.3, 5-F
1. 188
3-CH.sub.3, 4-Br
1. 189
3-CH.sub.3, 5-Br
1. 190
3-F, 4-CH.sub.3
1. 191
3-Cl, 4-CH.sub.3
1. 192
3-Br, 4-CH.sub.3
1. 193
2-Cl, 4,5-(CH.sub.3).sub.2
1. 194
2-Br, 4,5-(CH.sub.3).sub.2
1. 195
2-Cl, 3,5-(CH.sub.3).sub.2
1. 196
2-Br, 3,5-(CH.sub.3).sub.2
1. 197
2,6-Cl.sub.2, 4-CH.sub.3
1. 198
2,6-F.sub.2, 4-CH.sub.3
1. 199
2,6-Br.sub.2, 4-CH.sub.3
1. 200
2,4-Cl.sub.2, 6-CH.sub.3
1. 201
2,4-F.sub.2, 6-CH.sub.3
1. 202
2,4-Br.sub.2, 6-CH.sub.3
1. 203
2,6-(CH.sub.3).sub.2, 4-F
1. 204
2,6-(CH.sub.3).sub. 2, 4-Cl
94-97
2950, 1721, 1441, 1323, 1220, 1200, 1065, 1013
1. 205
2,6-(CH.sub.3).sub.2, 4-Br
resin
2950, 1722, 1436, 1321, 1220, 1199, 1067, 1014
1. 206
3,5-(CH.sub.3).sub.2, 4-F
1. 207
3,5-(CH.sub.3).sub.2, 4-Cl
1. 208
3,5-(CH.sub.3).sub.2, 4-Br
1. 209
2,3,6-(CH.sub.3).sub.3, 4-F
1. 210
2,3,6-(CH.sub.3).sub.3, 4-Cl
1. 211
2,3,6-(CH.sub.3).sub.3, 4-Br
1. 212
2,4-(CH.sub.3).sub.2, 6-F
1. 213
2,4-(CH.sub.3).sub.2, 6-Cl
1. 214
2,4-(CH.sub.3).sub.2, 6-Br
1. 215
2-i-C.sub.3 H.sub.7, 4-Cl, 5-CH.sub.3
oil 2960, 1727, 1495, 1437, 1245, 1219, 1170, 1124,
1070, 1019
1. 216
2-Cl, 4-NO.sub.2
1. 217
2-NO.sub.2, 4-Cl
1. 218
2-OCH.sub.3, 5-NO.sub.2
1. 219
2,4-Cl.sub.2, 5-NO.sub.2
1. 220
2,4-Cl.sub.2, 6-NO.sub.2
1. 221
2,6-Cl.sub.2, 4-NO.sub.2
1. 222
2,6-Br.sub.2, 4-NO.sub.2
1. 223
2,6-I.sub.2, 4-NO.sub.2
1. 224
2-CH.sub.3, 5-i-C.sub.3 H.sub.7, 4-Cl
oil 2962, 1727, 1492, 1437, 1255, 1217, 1165, 1069,
1047, 1020
1. 225
2-C.sub.6 H.sub.5 O
1. 226
3-C.sub.6 H.sub.5 O
1. 227
4-C.sub.6 H.sub.5 O
1. 228
3-t-C.sub.4 H.sub.9 O
1. 229
4-t-C.sub.4 H.sub.9 O
1. 230
*1) oil 2945, 1726, 1400, 1269, 1097, 1069, 1019, 771
1. 231
*2) oil 2950, 1727, 1441, 1214, 1177, 1066, 1012, 956
1. 232
4-OCH.sub.2 C.sub.6 H.sub.5
130-133
2955, 1728, 1504, 1231, 1204, 1069, 1016, 741
1. 233
2-OC.sub.2 H.sub.5
1. 234
2-CH.sub.3, 4-(1,1,3,3-tetramethylbutyl)
oil 2952, 2901, 1728, 1507, 1259, 1243, 1219, 1069,
1020
1. 235
2-Cl, 3-i-C.sub.3 H.sub.7
1. 236
2-CH.sub.3, 4-C.sub.6 H.sub.5
1. 237
4-(1,1,3-trimethylbutyl)
1. 238
3-CH.sub.3, 5-i-C.sub.3 H.sub.7
oil 2958, 1727, 1593, 1334, 1322, 1291, 1218, 1069,
1045, 1020
1. 239
2-CH.sub.3, 4-cyclo-C.sub.5 H.sub.9
1. 240
3-n-C.sub.4 H.sub.9 O
oil 1727, 1591, 1492, 1284, 1219, 1179, 1152, 1069,
1044, 1019
1. 241
4-n-C.sub.4 H.sub.9 O
66-67
1. 242
3-n-C.sub.6 H.sub.13 O
oil 2935, 1727, 1591, 1492, 1218, 1178, 1152, 1069,
1045, 1019
1. 243
4-n-C.sub.6 H.sub.13 O
69-70
1. 244
4-OC.sub.2 H.sub.5
64-66
1722, 1512, 1438, 1241, 1216, 1118, 1069, 1047,
1030
1. 245
2-OCH.sub.3, 4-CH.sub.3
oil 1727, 1512, 1464, 1301, 1265, 1221, 1157, 1141,
1069, 1018
1. 246
*3) 82-86
__________________________________________________________________________
##STR6##
##STR7##
##STR8##
TABLE 2
______________________________________
##STR9## (V)
mp
No. X.sub.m (°C.)
IR(cm.sup.-1)
______________________________________
2. 1 3-F
2. 2 4-F
2. 3 2,4-F.sub.2
2. 4 2,4,6-F.sub.3
2. 5 2,3,4,5,6-F.sub.5
2. 6 2,3-F.sub.2
2. 7 2,3-Cl.sub.2
2. 8 2,5-Cl.sub.2
2. 9 2,6-Cl.sub.2
2. 10 3,4-Cl.sub.2
2. 11 3,5-Cl.sub.2
2. 12 2,3,4-Cl.sub.3
2. 13 2,3,5-Cl.sub.3
2. 14 2,3,6-Cl.sub.3
2. 15 2,4,5-Cl.sub.3
2. 16 2,4,6-Cl.sub.3
2. 17 3,4,5-Cl.sub.3
2. 18 2,3,4,6-Cl.sub.4
2. 19 2,3,5,6-Cl.sub.4
2. 20 2,3,4,5,6-Cl.sub.5
2. 21 2-Br
2. 22 3-Br
2. 23 4-Br
2. 24 2,4-Br.sub.2
2. 25 2,5-Br.sub.2
2. 26 2,6-Br.sub.2
2. 27 2,4,6-Br.sub.3
2. 28 2,3,4,5,6-Br.sub.5
2. 29 2-I
2. 30 3-I
2. 31 4-I
2. 32 2,4-I.sub.2
2. 33 2-Cl, 3-F
2. 34 2-Cl, 4-F
2. 35 2-Cl, 5-F
2. 36 2-Cl, 6-F
2. 37 2-Cl, 3-Br
2. 38 2-Cl, 4-Br
2. 39 2-Cl, 5-Br
2. 40 2-Cl, 6-Br
2. 41 2-Br, 3-Cl
2. 42 2-Br, 4-Cl
2. 43 2-Br, 3-F
2. 45 2-Br, 4-F
2. 46 2-Br, 5-F
2. 47 2-Br, 6-F
2. 48 2-F, 3-Cl
2. 49 2-F, 4-Cl
2. 50 2-F, 5-Cl
2. 51 3-Cl, 4-F
2. 52 3-Cl, 5-F
2. 53 3-Cl, 4-Br
2. 54 3-Cl, 5-Br
2. 55 3-F, 4-Cl
2. 56 3-F, 4-Br
2. 57 3-Br, 4-Cl
2. 58 3-Br, 4-F
2. 59 2,6-Cl.sub.2, 4-Br
2. 60 3-CH.sub.3
2. 61 2,3-(CH.sub.3).sub.2
2. 62 2,4-(CH.sub.3).sub.2
70-71 1855, 1685, 1502,
1254, 1223, 1131,
1033, 805, 764
2. 63 2,5-(CH.sub.3).sub.2
2. 64 2,6-(CH.sub.3).sub.2
2. 65 3,4-(CH.sub.3).sub.2
2. 66 3,5-(CH.sub.3).sub.2
2. 67 2,3,4-(CH.sub.3).sub.3
2. 68 2,3,5-(CH.sub.3).sub.3
2. 69 2,3,6-(CH.sub.3).sub.3
2. 70 2,4,5-(CH.sub.3).sub.3
2. 71 2,4,6-(CH.sub.3).sub.3
2. 72 3,4,5-(CH.sub.3).sub.3
2. 73 2,3,4,6-(CH.sub.3).sub.4
2. 74 2,3,5,6-(CH.sub.3).sub.4
2. 75 2,3,4,5,6-(CH.sub.3).sub.5
2. 76 2-C.sub.2 H.sub.5
2. 77 3-C.sub.2 H.sub. 5
2. 78 4-C.sub.2 H.sub.5
2. 79 2,4-(C.sub.2 H.sub.5).sub.2
2. 80 2,6-(C.sub.2 H.sub.5).sub.2
2. 81 3,5-(C.sub.2 H.sub.5).sub.2
2. 82 2,4,6-(C.sub.2 H.sub.5).sub.3
2. 83 2-n-C.sub.3 H.sub.7
2. 84 3-n-C.sub.3 H.sub.7
2. 85 4-n-C.sub.3 H.sub.7
2. 86 2-i-C.sub.3 H.sub.7
2. 87 3-i-C.sub.3 H.sub.7
2. 88 4-i-C.sub.3 H.sub.7
2. 89 2,4-(i-C.sub.3 H.sub.7).sub.2
2. 90 2,6-(i-C.sub.3 H.sub.7).sub.2
2. 91 3,5-(i-C.sub.3 H.sub.7).sub.2
2. 92 2,4,6-(i-C.sub.3 H.sub.7).sub.3
2. 93 2-s-C.sub.4 H.sub.9
2. 94 3-s-C.sub.4 H.sub.9
2. 95 4-s-C.sub.4 H.sub.9
2. 96 2-t-C.sub.4 H.sub.9
2. 97 3-t-C.sub.4 H.sub.9
2. 98 2,3-(t-C.sub.4 H.sub.9).sub.2
2. 99 2,4-(t-C.sub.4 H.sub.9).sub.2
2. 100
2,5-(t-C.sub.4 H.sub.9).sub.2
2. 101
2,6-(t-C.sub.4 H.sub.9).sub.2
2. 102
3,5-(t-C.sub.4 H.sub.9).sub.2
2. 103
2,4,6-(t-C.sub.4 H.sub.9).sub.3
2. 104
4-n-C.sub.9 H.sub.19
2. 105
4-n-C.sub.12 H.sub.25
2. 106
3-n-C.sub. 15 H.sub.31
2. 107
4-(1,1,3,3-tetramethylbutyl)
2. 108
4-(2,3,3-trimethylpropyl)
2. 109
2-t-C.sub.4 H.sub.9, 4-CH.sub.3
2. 110
2-t-C.sub.4 H.sub.9, 5-CH.sub.3
2. 111
2,6-(t-C.sub.4 H.sub.9).sub.2, 4-CH.sub.3
2. 112
2-CH.sub.3, 4-t-C.sub.4 H.sub.9
2. 113
2-CH.sub.3, 6-t-C.sub.4 H.sub.9
2. 114
2-CH.sub.3, 4-i-C.sub.3 H.sub.7
2. 115
2-CH.sub.3, 5-i-C.sub.3 H.sub.7
2. 116
3-CH.sub.3, 4-i-C.sub.3 H.sub.7
2. 117
2-i-C.sub.3 H.sub.7, 5-CH.sub.3
2. 118
2,4-(t-C.sub.4 H.sub.9).sub.2, 6-i-C.sub.3 H.sub.7
2. 119
2-C.sub.3 H.sub.5 (= allyl)
2. 120
3-C.sub.3 H.sub.5
2. 121
4-C.sub.3 H.sub.5
2. 122
2-C.sub.3 H.sub.5, 6-CH.sub.3
2. 123
2-cyclo-C.sub.6 H.sub.11
2. 124
3-cyclo-C.sub.6 H.sub.11
2. 125
4-cyclo-C.sub.6 H.sub.11
2. 126
2,4-(cyclo-C.sub.6 H.sub.11).sub.2, 6-CH.sub.3
2. 127
2-CH.sub.3, 4-cyclo-C.sub.6 H.sub.11
2. 128
2-CH.sub.2 C.sub.6 H.sub.5
2. 129
3-CH.sub.2 C.sub.6 H.sub.5
2. 130
4-CH.sub.2 C.sub.6 H.sub.5
2. 131
2-CH.sub.2 C.sub.6 H.sub.5, 4-CH.sub.3
2. 132
2-CH.sub.3, 4-CH.sub.2 C.sub.6 H.sub.5
2. 133
2-C.sub.6 H.sub.5
2. 134
3-C.sub.6 H.sub.5
2. 135
4-C.sub.6 H.sub.5
2. 136
4-(2-i-C.sub.3 H.sub.7C.sub.6 H.sub.4)
2. 137
4-C.sub.6 H.sub.5, 2,6-(CH.sub.3).sub.2
2. 138
2-Cl, 4-C.sub.6 H.sub.5
2. 139
2-Br, 4-C.sub.6 H.sub.5
2. 140
2-C.sub.6 H.sub.5, 4-Cl
2. 141
2-C.sub.6 H.sub.5, 4-Br
2. 142
2-CH.sub.2 C.sub.6 H.sub.5, 4-Cl
2. 143
2-CH.sub.2 C.sub.6 H.sub.5, 4-Br
2. 144
2-Cl, 4-CH.sub.2 C.sub.6 H.sub.5
2. 145
2-Br, 4-CH.sub.2 C.sub.6 H.sub.5
2. 146
2-cyclo-C.sub.6 H.sub.11, 4-Cl
2. 147
2-cyclo-C.sub.6 H.sub.11, 4-Br
2. 148
2-Cl, 4-cyclo-C.sub.6 H.sub.11
2. 149
2-Br, 4-cyclo-C.sub.6 H.sub.11
2. 150
3-OCH.sub.3
2. 151
2,4-(OCH.sub.3).sub.2
2. 152
2-CF.sub.3
2. 153
3-CF.sub.3
2. 154
4-CF.sub.3
2. 155
2-OCF.sub.3
2. 156
3-OCF.sub.3
2. 157
4-OCF.sub.3
2. 158
3-OCH.sub.2 CHF.sub.2
2. 159
2-NO.sub.2
2. 160
3-NO.sub.2
2. 161
2-CN
2. 162
3-CN
2. 163
4-CN
2. 164
2-CH.sub.3, 3-Cl
2. 165
2-CH.sub.3, 5-Cl
2. 166
2-CH.sub.3, 6-Cl
2. 167
2-CH.sub.3, 3-F
2. 168
2-CH.sub.3, 4-F
2. 169
2-CH.sub.3, 5-F
2. 170
2-CH.sub.3, 6-F
2. 171
2-CH.sub.3, 3-Br
2. 172
2-CH.sub.3, 4-Br
2. 173
2-CH.sub.3, 5-Br
2. 174
2-CH.sub.3, 6-Br
2. 175
2-Cl, 3-CH.sub.3
2. 176
2-Cl, 4-CH.sub.3
2. 177
2-Cl, 5-CH.sub.3
2. 178
2-F, 3-CH.sub.3
2. 179
2-F, 4-CH.sub.3
2. 180
2-F, 5-CH.sub.3
2. 181
2-Br, 3-CH.sub.3
2. 182
2-Br, 4-CH.sub.3
2. 183
3-CH.sub.3, 4-Cl
2. 184
3-CH.sub.3, 5-Cl
2. 185
2-Br, 5-CH.sub.3
2. 186
3-CH.sub.3, 4-F
2. 187
3-CH.sub.3, 5-F
2. 188
3-CH.sub.3, 4-Br
2. 189
3-CH.sub.3, 5-Br
2. 190
3-F, 4-CH.sub.3
2. 191
3-Cl, 4-CH.sub.3
2. 192
3-Br, 4-CH.sub.3
2. 193
2-Cl, 4,5-(CH.sub.3).sub.2
2. 194
2-Br, 4,5-(CH.sub.3).sub.2
2. 195
2-Cl, 3,5-(CH.sub.3).sub.2
2. 196
2-Br, 3,5-(CH.sub.3).sub.2
2. 197
2,6-Cl.sub.2, 4-CH.sub.3
2. 198
2,6-F.sub.2, 4-CH.sub.3
2. 199
2,6-Br.sub.2, 4-CH.sub.3
2. 200
2,4-Cl.sub.2, 6-CH.sub.3
2. 201
2,4-F.sub.2, 6-CH.sub.3
2. 202
2,4-Br.sub.2, 6-CH.sub.3
2. 203
2,6-(CH.sub.3).sub.2, 4-F
2. 204
2,6-(CH.sub.3).sub.2, 4-Cl
2. 205
2,6-(CH.sub.3).sub.2, 4-Br
2. 206
3,5-(CH.sub.3).sub.2, 4-F
2. 207
3,5-(CH.sub.3).sub.2, 4-Cl
2. 208
3,5-(CH.sub.3).sub.2, 4-Br
2. 209
2,3,6-(CH.sub.3).sub.3, 4-F
2. 210
2,3,6-(CH.sub.3).sub.3, 4-Cl
2. 211
2,3,6-(CH.sub.3).sub.3, 4-Br
2. 212
2,4-(CH.sub.3).sub.2, 6-F
2. 213
2,4-(CH.sub.3).sub.2, 6-Cl
2. 214
2,4-(CH.sub.3).sub.2, 6-Br
2. 215
2-i-C.sub.3 H.sub.7, 4-Cl, 5-CH.sub.3
2. 216
2-Cl, 4-NO.sub.2
2. 217
2-NO.sub.2, 4-Cl
2. 218
2-OCH.sub.3, 5-NO.sub.2
2. 219
2,4-Cl.sub.2, 5-NO.sub.2
2. 220
2,4-Cl.sub.2, 6-NO.sub.2
2. 221
2,6-Cl.sub.2, 4-NO.sub.2
2. 222
2,6-Br.sub.2, 4-NO.sub.2
2. 223
2,6-I.sub.2, 4-NO.sub.2
2. 224
2-CH.sub.3, 5-i-C.sub.3 H.sub.7, 4-Cl
2. 225
2-C.sub.6 H.sub.5 O
2. 226
3-C.sub.6 H.sub.5 O
2. 227
4-C.sub.6 H.sub.5 O
2. 228
3-t-C.sub.4 H.sub.9 O
2. 229
4-t-C.sub.4 H.sub.9 O
2. 230
*1)
2. 231
*2)
______________________________________
##STR10##
##STR11##
TABLE 3
______________________________________
##STR12## (IV)
mp
No. X.sub.m (°C.)
IR(cm.sup.-1)
______________________________________
3. 1 3-F
3. 2 4-F
3. 3 2,4-F.sub.2
3. 4 2,4,6-F.sub.3
3. 5 2,3,4,5,6-F.sub.5
3. 6 2,3-F.sub.2
3. 7 2,3-Cl.sub.2
3. 8 2,5-Cl.sub.2
3. 9 2,6-Cl.sub.2
3. 10 3,4-Cl.sub.2
3. 11 3,5-Cl.sub.2
3. 12 2,3,4-Cl.sub.3
3. 13 2,3,5-Cl.sub.3
3. 14 2,3,6-Cl.sub.3
3. 15 2,4,5-Cl.sub.3
3. 16 2,4,6-Cl.sub.3
3. 17 3,4,5-Cl.sub.3
3. 18 2,3,4,6-Cl.sub.4
3. 19 2,3,5,6-Cl.sub.4
3. 20 2,3,4,5,6-Cl.sub.5
3. 21 2-Br
3. 22 3-Br
3. 23 4-Br
3. 24 2,4-Br.sub.2
3. 25 2,5-Br.sub.2
3. 26 2,6-Br.sub.2
3. 27 2,4,6-Br.sub.3
3. 28 2,3,4,5,6-Br.sub.5
3. 29 2-I
3. 30 3-I
3. 31 4-I
3. 32 2,4-I.sub.2
3. 33 2-Cl, 3-F
3. 34 2-Cl, 4-F
3. 35 2-Cl, 5-F
3. 36 2-Cl, 6-F
3. 37 2-Cl, 3-Br
3. 38 2-Cl, 4-Br
3. 39 2-Cl, 5-Br
3. 40 2-Cl, 6-Br
3. 41 2-Br, 3-Cl
3. 42 2-Br, 4-Cl
3. 43 2-Br, 3-F
3. 45 2-Br, 4-F
3. 46 2-Br, 5-F
3. 47 2-Br, 6-F
3. 48 2-F, 3-Cl
3. 49 2-F, 4-Cl
3. 50 2-F, 5-Cl
3. 51 3-Cl, 4-F
3. 52 3-Cl, 5-F
3. 53 3-Cl, 4-Br
3. 54 3-Cl, 5-Br
3. 55 3-F, 4-Cl
3. 56 3-F, 4-Br
3. 57 3-Br, 4-Cl
3. 58 3-Br, 4-F
3. 59 2,6-Cl.sub.2, 4-Br
3. 60 3-CH.sub.3
3. 61 2,3-(CH.sub.3).sub.2
3. 62 2,4-(CH.sub.3).sub.2
oil 3422, 2910, 1504, 1255,
1220, 1133, 1035, 759
3. 63 2,5-(CH.sub.3).sub.2
3. 64 2,6-(CH.sub.3).sub.2
3. 65 3,4-(CH.sub.3).sub.2
3. 66 3,5-(CH.sub.3).sub.2
3. 67 2,3,4-(CH.sub.3).sub.3
3. 68 2,3,5-(CH.sub.3).sub.3
3. 69 2,3,6-(CH.sub.3).sub.3
3. 70 2,4,5-(CH.sub.3).sub.3
3. 71 2,4,6-(CH.sub.3).sub.3
3. 72 3,4,5-(CH.sub.3).sub.3
3. 73 2,3,4,6-(CH.sub.3).sub.4
3. 74 2,3,5,6-(CH.sub.3).sub.4
3. 75 2,3,4,5,6-(CH.sub.3).sub.5
3. 76 2-C.sub.2 H.sub.5
3. 77 3-C.sub.2 H.sub.5
3. 78 4-C.sub.2 H.sub.5
3. 79 2,4-(C.sub.2 H.sub.5).sub.2
3. 80 2,6-(C.sub.2 H.sub.5).sub.2
3. 81 3,5-(C.sub.2 H.sub.5).sub.2
3. 82 2,4,6-(C.sub.2 H.sub.5).sub.3
3. 83 2-n-C.sub.3 H.sub.7
3. 84 3-n-C.sub.3 H.sub.7
3. 85 4-n-C.sub.3 H.sub.7
3. 86 2-i-C.sub.3 H.sub.7
3. 87 3-i-C.sub.3 H.sub.7
3. 88 4-i-C.sub.3 H.sub.7
3. 89 2,4-(i-C.sub.3 H.sub.7).sub.2
3. 90 2,6-(i-C.sub.3 H.sub.7).sub.2
3. 91 3,5-(i-C.sub.3 H.sub.7).sub.2
3. 92 2,4,6-(i-C.sub.3 H.sub.7).sub.3
3. 93 2-s-C.sub.4 H.sub.9
3. 94 3-s-C.sub.4 H.sub.9
3. 95 4-s-C.sub.4 H.sub.9
3. 96 2-t-C.sub.4 H.sub.9
3. 97 3-t-C.sub.4 H.sub.9
3. 98 2,3-(t-C.sub.4 H.sub.9).sub.2
3. 99 2,4-(t-C.sub.4 H.sub.9).sub.2
3. 100
2,5-(t-C.sub.4 H.sub.9).sub.2
3. 101
2,6-(t-C.sub.4 H.sub.9).sub.2
3. 102
3,5-(t-C.sub.4 H.sub.9).sub.2
3. 103
2,4,6-(t-C.sub.4 H.sub.9).sub.3
3. 104
4-n-C.sub.9 H.sub.19
3. 105
4-n-C.sub.12 H.sub.25
3. 106
3-n-C.sub.15 H.sub.31
3. 107
4-(1,1,3,3-tetramethylbutyl)
3. 108
4-(2,3,3-trimethylpropyl)
3. 109
2-t-C.sub.4 H.sub.9, 4-CH.sub.3
3. 110
2-t-C.sub.4 H.sub.9, 5-CH.sub.3
3. 111
2,6-(t-C.sub.4 H.sub.9).sub.2, 4-CH.sub.3
3. 112
2-CH.sub.3, 4-t-C.sub.4 H.sub.9
3. 113
2-CH.sub.3, 6-t-C.sub.4 H.sub.9
3. 114
2-CH.sub.3, 4-i-C.sub.3 H.sub.7
3. 115
2-CH.sub.3, 5-i-C.sub.3 H.sub.7
3. 116
3-CH.sub.3, 4-i-C.sub.3 H.sub.7
3. 117
2-i-C.sub.3 H.sub.7, 5-CH.sub.3
3. 118
2,4-(t-C.sub.4 H.sub.9).sub.2, 6-i-C.sub.3 H.sub.7
3. 119
2-C.sub.3 H.sub.5 (= allyl)
3. 120
3-C.sub.3 H.sub.5
3. 121
4-C.sub.3 H.sub.5
3. 122
2-C.sub.3 H.sub.5, 6-CH.sub.3
3. 123
2-cyclo-C.sub.6 H.sub.11
3. 124
3-cyclo-C.sub.6 H.sub.11
3. 125
4-cyclo-C.sub.6 H.sub.11
3. 126
2,4-(cyclo-C.sub.6 H.sub.11).sub.2, 6-CH.sub.3
3. 127
2-CH.sub.3, 4-cyclo-C.sub.6 H.sub.11
3. 128
2-CH.sub.2 C.sub.6 H.sub.5
3. 129
3-CH.sub.2 C.sub.6 H.sub.5
3. 130
4-CH.sub.2 C.sub.6 H.sub.5
3. 131
2-CH.sub.2 C.sub.6 H.sub.5, 4-CH.sub.3
3. 132
2-CH.sub.3, 4-CH.sub.2 C.sub.6 H.sub.5
3. 133
2-C.sub.6 H.sub.5
3. 134
3-C.sub.6 H.sub.5
3. 135
4-C.sub.6 H.sub.5
3. 136
4-(2-i-C.sub.3 H.sub.7C.sub.6 H.sub.4)
3. 137
4-C.sub.6 H.sub.5, 2,6-(CH.sub.3).sub.2
3. 138
2-Cl, 4-C.sub.6 H.sub.5
3. 139
2-Br, 4-C.sub.6 H.sub.5
3. 140
2-C.sub.6 H.sub.5, 4-Cl
3. 141
2-C.sub.6 H.sub.5, 4-Br
3. 142
2-CH.sub.2 C.sub.6 H.sub.5, 4-Cl
3. 143
2-CH.sub.2 C.sub.6 H.sub.5, 4-Br
3. 144
2-Cl, 4-CH.sub.2 C.sub.6 H.sub.5
3. 145
2-Br, 4-CH.sub.2 C.sub.6 H.sub.5
3. 146
2-cyclo-C.sub.6 H.sub.11, 4-Cl
3. 147
2-cyclo-C.sub.6 H.sub.11, 4-Br
3. 148
2-Cl, 4-cyclo-C.sub.6 H.sub.11
3. 149
2-Br, 4-cyclo-C.sub.6 H.sub.11
3. 150
3-OCH.sub.3
3. 151
2,4-(OCH.sub.3).sub.2
3. 152
2-CF.sub.3
3. 153
3-CF.sub.3
3. 154
4-CF.sub.3
3. 155
2-OCF.sub.3
3. 156
3-OCF.sub.3
3. 157
4-OCF.sub. 3
3. 158
3-OCH.sub.2 CHF.sub.2
3. 159
2-NO.sub.2
3. 160
3-NO.sub.2
3. 161
2-CN
3. 162
3-CN
3. 163
4-CN
3. 164
2-CH.sub.3, 3-Cl
3. 165
2-CH.sub.3, 5-Cl
3. 166
2-CH.sub.3, 6-Cl
3. 167
2-CH.sub.3, 3-F
3. 168
2-CH.sub.3, 4-F
3. 169
2-CH.sub.3, 5-F
3. 170
2-CH.sub.3, 6-F
3. 171
2-CH.sub.3, 3-Br
3. 172
2-CH.sub.3, 4-Br
3. 173
2-CH.sub.3, 5-Br
3. 174
2-CH.sub.3, 6-Br
3. 175
2-Cl, 3-CH.sub.3
3. 176
2-Cl, 4-CH.sub.3
3. 177
2-Cl, 5-CH.sub.3
3. 178
2-F, 3-CH.sub.3
3. 179
2-F, 4-CH.sub.3
3. 180
2-F, 5-CH.sub.3
3. 181
2-Br, 3-CH.sub.3
3. 182
2-Br, 4-CH.sub.3
3. 183
3-CH.sub.3, 4-Cl
3. 184
3-CH.sub.3, 5-Cl
3. 185
2-Br, 5-CH.sub.3
3. 186
3-CH.sub.3, 4-F
3. 187
3-CH.sub.3, 5-F
3. 188
3-CH.sub.3, 4-Br
3. 189
3-CH.sub.3, 5-Br
3. 190
3-F, 4-CH.sub.3
3. 191
3-Cl, 4-CH.sub.3
3. 192
3-Br, 4-CH.sub.3
3. 193
2-Cl, 4,5-(CH.sub.3).sub.2
3. 194
2-Br, 4,5-(CH.sub.3).sub.2
3. 195
2-Cl, 3,5-(CH.sub.3).sub.2
3. 196
2-Br, 3,5-(CH.sub.3).sub.2
3. 197
2,6-Cl.sub.2, 4-CH.sub.3
3. 198
2,6-F.sub.2, 4-CH.sub.3
3. 199
2,6-Br.sub.2, 4-CH.sub.3
3. 200
2,4-Cl.sub.2, 6-CH.sub.3
3. 201
2,4-F.sub.2, 6-CH.sub.3
3. 202
2,4-Br.sub.2, 6-CH.sub.3
3. 203
2,6-(CH.sub.3).sub.2, 4-F
3. 204
2,6-(CH.sub.3).sub.2, 4-Cl
3. 205
2,6-(CH.sub.3).sub.2, 4-Br
3. 206
3,5-(CH.sub.3).sub.2, 4-F
3. 207
3,5-(CH.sub.3).sub.2, 4-Cl
3. 208
3,5-(CH.sub.3).sub.2, 4-Br
3. 209
2,3,6-(CH.sub.3).sub.3, 4-F
3. 210
2,3,6-(CH.sub.3).sub.3, 4-Cl
3. 211
2,3,6-(CH.sub.3).sub.3, 4-Br
3. 212
2,4-(CH.sub.3).sub.2, 6-F
3. 213
2,4-(CH.sub.3).sub.2, 6-Cl
3. 214
2,4-(CH.sub.3).sub.2, 6-Br
3. 215
2-i-C.sub.3 H.sub.7, 4-Cl, 5-CH.sub.3
3. 216
2-Cl, 4-NO.sub.2
3. 217
2-NO.sub.2, 4-Cl
3. 218
2-OCH.sub.3, 5-NO.sub.2
3. 219
2,4-Cl.sub.2, 5-NO.sub.2
3. 220
2,4-Cl.sub.2, 6-NO.sub.2
3. 221
2,6-Cl.sub.2, 4-NO.sub. 2
3. 222
2,6-Br.sub.2, 4-NO.sub.2
3. 223
2,6-I.sub.2, 4-NO.sub.2
3. 224
2-CH.sub.3, 5-i-C.sub.3 H.sub.7, 4-Cl
3. 225
2-C.sub.6 H.sub.5 O
3. 226
3-C.sub.6 H.sub.5 O
3. 227
4-C.sub.6 H.sub.5 O
3. 228
3-t-C.sub.4 H.sub.9 O
3. 229
4-t-C.sub.4 H.sub.9 O
3. 230
*1)
3. 231
*2)
______________________________________
##STR13##
##STR14##
TABLE 4
______________________________________
##STR15## (III)
mp
No. X.sub.m (°C.)
IR(cm.sup.-1)
______________________________________
4. 1 3-F
4. 2 4-F
4. 3 2,4-F.sub.2
4. 4 2,4,6-F.sub.3
4. 5 2,3,4,5,6-F.sub.5
4. 6 2,3-F.sub.2
4. 7 2,3-Cl.sub.2
4. 8 2,5-Cl.sub.2
4. 9 2,6-Cl.sub.2
4. 10 3,4-Cl.sub.2
4. 11 3,5-Cl.sub.2
4. 12 2,3,4-Cl.sub.3
4. 13 2,3,5-Cl.sub.3
4. 14 2,3,6-Cl.sub.3
4. 15 2,4,5-Cl.sub.3
4. 16 2,4,6-Cl.sub.3
4. 17 3,4,5-Cl.sub.3
4. 18 2,3,4,6-Cl.sub.4
4. 19 2,3,5,6-Cl.sub.4
4. 20 2,3,4,5,6-Cl.sub.5
4. 21 2-Br
4. 22 3-Br
4. 23 4-Br
4. 24 2,4-Br.sub.2
4. 25 2,5-Br.sub.2
4. 26 2,6-Br.sub.2
4. 27 2,4,6-Br.sub.3
4. 28 2,3,4,5,6-Br.sub.5
4. 29 2-I
4. 30 3-I
4. 31 4-I
4. 32 2,4-I.sub.2
4. 33 2-Cl, 3-F
4. 34 2-Cl, 4-F
4. 35 2-Cl, 5-F
4. 36 2-Cl, 6-F
4. 37 2-Cl, 3-Br
4. 38 2-Cl, 4-Br
4. 39 2-Cl, 5-Br
4. 40 2-Cl, 6-Br
4. 41 2-Br, 3-Cl
4. 42 2-Br, 4-Cl
4. 43 2-Br, 3-F
4. 45 2-Br, 4-F
4. 46 2-Br, 5-F
4. 47 2-Br, 6-F
4. 48 2-F, 3-Cl
4. 49 2-F, 4-Cl
4. 50 2-F, 5-Cl
4. 51 3-Cl, 4-F
4. 52 3-Cl, 5-F
4. 53 3-Cl, 4-Br
4. 54 3-Cl, 5-Br
4. 55 3-F, 4-Cl
4. 56 3-F, 4-Br
4. 57 3-Br, 4-Cl
4. 58 3-Br, 4-F
4. 59 2,6-Cl.sub.2, 4-Br
4. 60 3-CH.sub.3
4. 61 2,3-(CH.sub.3).sub.2
4. 62 2,4-(CH.sub.3).sub.2
oil 3460, 2915, 1739, 1503,
1254, 1221
4. 63 2,5-(CH.sub.3).sub.2
4. 64 2,6-(CH.sub.3).sub.2
4. 65 3,4-(CH.sub.3).sub.2
4. 66 3,5-(CH.sub.3).sub.2
4. 67 2,3,4-(CH.sub.3).sub.3
4. 68 2,3,5-(CH.sub.3).sub.3
4. 69 2,3,6-(CH.sub.3).sub.3
4. 70 2,4,5-(CH.sub.3).sub.3
4. 71 2,4,6-(CH.sub.3).sub.3
4. 72 3,4,5-(CH.sub.3).sub.3
4. 73 2,3,4,6-(CH.sub.3).sub.4
4. 74 2,3,5,6-(CH.sub.3).sub.4
4. 75 2,3,4,5,6-(CH.sub.3).sub.5
4. 76 2-C.sub.2 H.sub.5
4. 77 3-C.sub.2 H.sub.5
4. 78 4-C.sub.2 H.sub.5
4. 79 2,4-(C.sub.2 H.sub.5).sub.2
4. 80 2,6-(C.sub.2 H.sub.5).sub.2
4. 81 3,5-(C.sub.2 H.sub.5).sub.2
4. 82 2,4,6-(C.sub.2 H.sub.5).sub.3
4. 83 2-n-C.sub.3 H.sub.7
4. 84 3-n-C.sub.3 H.sub.7
4. 85 4-n-C.sub.3 H.sub.7
4. 86 2-i-C.sub.3 H.sub.7
4. 87 3-i-C.sub.3 H.sub.7
4. 88 4-i-C.sub.3 H.sub.7
4. 89 2,4-(i-C.sub.3 H.sub.7).sub.2
4. 90 2,6-(i-C.sub.3 H.sub.7).sub.2
4. 91 3,5-(i-C.sub.3 H.sub.7).sub.2
4. 92 2,4,6-(i-C.sub.3 H.sub.7).sub.3
4. 93 2-s-C.sub.4 H.sub.9
4. 94 3-s-C.sub.4 H.sub.9
4. 95 4-s-C.sub.4 H.sub.9
4. 96 2-t-C.sub.4 H.sub.9
4. 97 3-t-C.sub.4 H.sub.9
4. 98 2,3-(t-C.sub.4 H.sub.9).sub.2
4. 99 2,4-(t-C.sub.4 H.sub.9).sub.2
4. 100
2,5-(t-C.sub.4 H.sub.9).sub.2
4. 101
2,6-(t-C.sub.4 H.sub.9).sub.2
4. 102
3,5-(t-C.sub.4 H.sub.9).sub.2
4. 103
2,4,6-(t-C.sub.4 H.sub.9).sub.3
4. 104
4-n-C.sub.9 H.sub.19
4. 105
4-n-C.sub.12 H.sub.25
4. 106
3-n-C.sub.15 H.sub.31
4. 107
4-(1,1,3,3-tetramethylbutyl)
4. 108
4-(2,3,3-trimethylpropyl)
4. 109
2-t-C.sub.4 H.sub.9, 4-CH.sub.3
4. 110
2-t-C.sub.4 H.sub.9, 5-CH.sub.3
4. 111
2,6-(t-C.sub.4 H.sub.9).sub.2, 4-CH.sub.3
4. 112
2-CH.sub.3, 4-t-C.sub.4 H.sub.9
4. 113
2-CH.sub.3, 6-t-C.sub.4 H.sub.9
4. 114
2-CH.sub.3, 4-i-C.sub.3 H.sub.7
4. 115
2-CH.sub.3, 5-i-C.sub.3 H.sub.7
4. 116
3-CH.sub.3, 4-i-C.sub.3 H.sub.7
4. 117
2-i-C.sub.3 H.sub.7, 5-CH.sub.3
4. 118
2,4-(t-C.sub.4 H.sub.9).sub.2, 6-i-C.sub.3 H.sub.7
4. 119
2-C.sub.3 H.sub.5 (= allyl)
4. 120
3-C.sub.3 H.sub.5
4. 121
4-C.sub.3 H.sub.5
4. 122
2-C.sub.3 H.sub.5, 6-CH.sub.3
4. 123
2-cyclo-C.sub.6 H.sub.11
4. 124
3-cyclo-C.sub.6 H.sub.11
4. 125
4-cyclo-C.sub.6 H.sub.11
4. 126
2,4-(cyclo-C.sub.6 H.sub.11).sub.2, 6-CH.sub.3
4. 127
2-CH.sub.3, 4-cyclo-C.sub.6 H.sub.11
4. 128
2-CH.sub.2 C.sub.6 H.sub.5
4. 129
3-CH.sub.2 C.sub.6 H.sub.5
4. 130
4-CH.sub.2 C.sub.6 H.sub.5
4. 131
2-CH.sub. 2 C.sub.6 H.sub.5, 4-CH.sub.3
4. 132
2-CH.sub.3, 4-CH.sub.2 C.sub.6 H.sub.5
4. 133
2-C.sub.6 H.sub.5
4. 134
3-C.sub.6 H.sub.5
4. 135
4-C.sub.6 H.sub.5
4. 136
4-(2-i-C.sub.3 H.sub.7C.sub.6 H.sub.4)
4. 137
4-C.sub.6 H.sub.5, 2,6-(CH.sub.3).sub.2
4. 138
2-Cl, 4-C.sub.6 H.sub.5
4. 139
2-Br, 4-C.sub.6 H.sub.5
4. 140
2-C.sub.6 H.sub.5, 4-Cl
4. 141
2-C.sub.6 H.sub.5, 4-Br
4. 142
2-CH.sub.2 C.sub.6 H.sub.5, 4-Cl
4. 143
2-CH.sub.2 C.sub.6 H.sub.5, 4-Br
4. 144
2-Cl, 4-CH.sub.2 C.sub.6 H.sub.5
4. 145
2-Br, 4-CH.sub.2 C.sub.6 H.sub.5
4. 146
2-cyclo-C.sub.6 H.sub.11, 4-Cl
4. 147
2-cyclo-C.sub.6 H.sub.11, 4-Br
4. 148
2-Cl, 4-cyclo-C.sub.6 H.sub.11
4. 149
2-Br, 4-cyclo-C.sub.6 H.sub.11
4. 150
3-OCH.sub.3
4. 151
2,4-(OCH.sub.3).sub.2
4. 152
2-CF.sub.3
4. 153
3-CF.sub.3
4. 154
4-CF.sub.3
4. 155
2-OCF.sub.3
4. 156
3-OCF.sub.3
4. 157
4-OCF.sub.3
4. 158
3-OCH.sub.2 CHF.sub.2
4. 159
2-NO.sub. 2
4. 160
3-NO.sub.2
4. 161
2-CN
4. 162
3-CN
4. 163
4-CN
4. 164
2-CH.sub.3, 3-Cl
4. 165
2-CH.sub.3, 5-Cl
4. 166
2-CH.sub.3, 6-Cl
4. 167
2-CH.sub.3, 3-F
4. 168
2-CH.sub.3, 4-F
4. 169
2-CH.sub.3, 5-F
4. 170
2-CH.sub.3, 6-F
4. 171
2-CH.sub.3, 3-Br
4. 172
2-CH.sub.3, 4-Br
4. 173
2-CH.sub.3, 5-Br
4. 174
2-CH.sub.3, 6-Br
4. 175
2-Cl, 3-CH.sub.3
4. 176
2-Cl, 4-CH.sub.3
4. 177
2-Cl, 5-CH.sub.3
4. 178
2-F, 3-CH.sub.3
4. 179
2-F, 4-CH.sub.3
4. 180
2-F, 5-CH.sub.3
4. 181
2-Br, 3-CH.sub.3
4. 182
2-Br, 4-CH.sub.3
4. 183
3-CH.sub.3, 4-Cl
4. 184
3-CH.sub.3, 5-Cl
4. 185
2-Br, 5-CH.sub.3
4. 186
3-CH.sub.3, 4-F
4. 187
3-CH.sub.3, 5-F
4. 188
3-CH.sub.3, 4-Br
4. 189
3-CH.sub.3, 5-Br
4. 190
3-F, 4-CH.sub.3
4. 191
3-Cl, 4-CH.sub.3
4. 192
3-Br, 4-CH.sub.3
4. 193
2-Cl, 4,5-(CH.sub.3).sub.2
4. 194
2-Br, 4,5-(CH.sub.3).sub.2
4. 195
2-Cl, 3,5-(CH.sub.3).sub.2
4. 196
2-Br, 3,5-(CH.sub.3).sub.2
4. 197
2,6-Cl.sub.2, 4-CH.sub.3
4. 198
2,6-F.sub.2, 4-CH.sub.3
4. 199
2,6-Br.sub.2, 4-CH.sub.3
4. 200
2,4-Cl.sub.2, 6-CH.sub.3
4. 201
2,4-F.sub.2, 6-CH.sub.3
4. 202
2,4-Br.sub.2, 6-CH.sub.3
4. 203
2,6-(CH.sub.3).sub.2, 4-F
4. 204
2,6-(CH.sub.3).sub.2, 4-Cl
4. 205
2,6-(CH.sub.3).sub.2, 4-Br
4. 206
3,5-(CH.sub.3).sub.2, 4-F
4. 207
3,5-(CH.sub.3).sub.2, 4-Cl
4. 208
3,5-(CH.sub.3).sub.2, 4-Br
4. 209
2,3,6-(CH.sub.3).sub.3, 4-F
4. 210
2,3,6-(CH.sub.3).sub.3, 4-Cl
4. 211
2,3,6-(CH.sub.3).sub.3, 4-Br
4. 212
2,4-(CH.sub.3).sub.2, 6-F
4. 213
2,4-(CH.sub.3).sub.2, 6-Cl
4. 214
2,4-(CH.sub.3).sub.2, 6-Br
4. 215
2-i-C.sub.3 H.sub.7, 4-Cl, 5-CH.sub.3
4. 216
2-Cl, 4-NO.sub.2
4. 217
2-NO.sub.2, 4-Cl
4. 218
2-OCH.sub.3, 5-NO.sub.2
4. 219
2,4-Cl.sub.2, 5-NO.sub.2
4. 220
2,4-Cl.sub.2, 6-NO.sub.2
4. 221
2,6-Cl.sub.2, 4-NO.sub.2
4. 222
2,6-Br.sub.2, 4-NO.sub.2
4. 223
2,6-I.sub.2, 4-NO.sub.2
4. 224
2-CH.sub.3, 5-i-C.sub.3 H.sub.7, 4-Cl
4. 225
2-C.sub.6 H.sub.5 O
4. 226
3-C.sub.6 H.sub.5 O
4. 227
4-C.sub.6 H.sub.5 O
4. 228
3-t-C.sub.4 H.sub.9 O
4. 229
4-t-C.sub.4 H.sub.9 O
4. 230
*1)
4. 231
*2)
______________________________________
##STR16##
##STR17##
TABLE 5
______________________________________
##STR18## (II)
mp
No. X.sub.m (°C.)
IR(cm.sup.-1)
______________________________________
5. 1 3-F
5. 2 4-F
5. 3 2,4-F.sub.2
5. 4 2,4,6-F.sub.3
5. 5 2,3,4,5,6-F.sub.5
5. 6 2,3-F.sub.2
5. 7 2,3-Cl.sub.2
5. 8 2,5-Cl.sub.2
5. 9 2,6-Cl.sub.2
5. 10 3,4-Cl.sub.2
5. 11 3,5-Cl.sub.2
5. 12 2,3,4-Cl.sub.3
5. 13 2,3,5-Cl.sub.3
5. 14 2,3,6-Cl.sub.3
5. 15 2,4,5-Cl.sub.3
5. 16 2,4,6-Cl.sub.3
5. 17 3,4,5-Cl.sub.3
5. 18 2,3,4,6-Cl.sub.4
5. 19 2,3,5,6-Cl.sub.4
5. 20 2,3,4,5,6-Cl.sub.5
5. 21 2-Br
5. 22 3-Br
5. 23 4-Br
5. 24 2,4-Br.sub.2
5. 25 2,5-Br.sub.2
5. 26 2,6-Br.sub.2
5. 27 2,4,6-Br.sub.3
5. 28 2,3,4,5,6-Br.sub.5
5. 29 2-I
5. 30 3-I
5. 31 4-I
5. 32 2,4-I.sub.2
5. 33 2-Cl, 3-F
5. 34 2-Cl, 4-F
5. 35 2-Cl, 5-F
5. 36 2-Cl, 6-F
5. 37 2-Cl, 3-Br
5. 38 2-Cl, 4-Br
5. 39 2-Cl, 5-Br
5. 40 2-Cl, 6-Br
5. 41 2-Br, 3-Cl
5. 42 2-Br, 4-Cl
5. 43 2-Br, 3-F
5. 45 2-Br, 4-F
5. 46 2-Br, 5-F
5. 47 2-Br, 6-F
5. 48 2-F, 3-Cl
5. 49 2-F, 4-Cl
5. 50 2-F, 5-Cl
5. 51 3-Cl, 4-F
5. 52 3-Cl, 5-F
5. 53 3-Cl, 4-Br
5. 54 3-Cl, 5-Br
5. 55 3-F, 4-Cl
5. 56 3-F, 4-Br
5. 57 3-Br, 4-Cl
5. 58 3-Br, 4-F
5. 59 2,6-Cl.sub.2, 4-Br
5. 60 3-CH.sub.3 1732, 1699, 1601, 1258,
1204, 1156, 760
5. 61 2,3-(CH.sub.3).sub.2
5. 62 2,4-(CH.sub.3).sub.2 1734, 1678, 1505, 1258,
1207, 1137, 1007, 796
5. 63 2,5-(CH.sub.3).sub.2
5. 64 2,6-(CH.sub.3).sub.2
5. 65 3,4-(CH.sub.3).sub.2
5. 66 3,5-(CH.sub.3).sub.2
5. 67 2,3,4-(CH.sub.3).sub.3
5. 68 2,3,5-(CH.sub.3).sub.3
5. 69 2,3,6-(CH.sub.3).sub.3
5. 70 2,4,5-(CH.sub.3).sub.3
5. 71 2,4,6-(CH.sub.3).sub.3
5. 72 3,4,5-(CH.sub.3).sub.3
5. 73 2,3,4,6-(CH.sub.3).sub.4
5. 74 2,3,5,6-(CH.sub.3).sub.4
5. 75 2,3,4,5,6-(CH.sub.3).sub.5
5. 76 2-C.sub.2 H.sub.5
5. 77 3-C.sub.2 H.sub.5
5. 78 4-C.sub.2 H.sub.5
5. 79 2,4-(C.sub.2 H.sub.5).sub.2
5. 80 2,6-(C.sub.2 H.sub.5).sub.2
5. 81 3,5-(C.sub.2 H.sub.5).sub.2
5. 82 2,4,6-(C.sub.2 H.sub.5).sub.3
5. 83 2-n-C.sub.3 H.sub.7
5. 84 3-n-C.sub.3 H.sub.7
5. 85 4-n-C.sub.3 H.sub.7
5. 86 2-i-C.sub.3 H.sub.7
5. 87 3-i-C.sub.3 H.sub.7
5. 88 4-i-C.sub.3 H.sub.7
5. 89 2,4-(i-C.sub.3 H.sub.7).sub.2
5. 90 2,6-(i-C.sub.3 H.sub.7).sub.2
5. 91 3,5-(i-C.sub.3 H.sub.7).sub.2
5. 92 2,4,6-(i-C.sub.3 H.sub.7).sub.3
5. 93 2-s-C.sub.4 H.sub.9
5. 94 3-s-C.sub.4 H.sub.9
5. 95 4-s-C.sub.4 H.sub.9
5. 96 2-t-C.sub.4 H.sub.9
5. 97 3-t-C.sub.4 H.sub.9
5. 98 2,3-(t-C.sub.4 H.sub.9).sub.2
5. 99 2,4-(t-C.sub.4 H.sub.9).sub.2
5. 100
2,5-(t-C.sub.4 H.sub.9).sub.2
5. 101
2,6-(t-C.sub.4 H.sub.9).sub.2
5. 102
3,5-(t-C.sub.4 H.sub.9).sub.2
5. 103
2,4,6-(t-C.sub.4 H.sub.9).sub.3
5. 104
4-n-C.sub.9 H.sub.19
5. 105
4-n-C.sub.12 H.sub.25
5. 106
3-n-C.sub.15 H.sub.31
5. 107
4-(1,1,3,3-tetramethylbutyl)
5. 108
4-(2,3,3-trimethylpropyl)
5. 109
2-t-C.sub.4 H.sub.9, 4-CH.sub.3
5. 110
2-t-C.sub.4 H.sub.9, 5-CH.sub.3
5. 111
2,6-(t-C.sub.4 H.sub.9).sub.2, 4-CH.sub.3
5. 112
2-CH.sub.3, 4-t-C.sub.4 H.sub.9
5. 113
2-CH.sub.3, 6-t-C.sub.4 H.sub.9
5. 114
2-CH.sub.3, 4-i-C.sub.3 H.sub.7
5. 115
2-CH.sub.3, 5-i-C.sub.3 H.sub.7
5. 116
3-CH.sub.3, 4-i-C.sub.3 H.sub.7
5. 117
2-i-C.sub.3 H.sub.7, 5-CH.sub.3
5. 118
2,4-(t-C.sub.4 H.sub.9).sub.2, 6-i-C.sub.3 H.sub.7
5. 119
2-C.sub.3 H.sub.5 (= allyl)
5. 120
3-C.sub.3 H.sub.5
5. 121
4-C.sub.3 H.sub.5
5. 122
2-C.sub.3 H.sub.5, 6-CH.sub.3
5. 123
2-cyclo-C.sub.6 H.sub.11
5. 124
3-cyclo-C.sub.6 H.sub.11
5. 125
4-cyclo-C.sub.6 H.sub.11
5. 126
2,4-(cyclo-C.sub.6 H.sub.11).sub.2, 6-CH.sub.3
5. 127
2-CH.sub.3, 4-cyclo-C.sub.6 H.sub.11
5. 128
2-CH.sub.2 C.sub.6 H.sub.5
5. 129
3-CH.sub. 2 C.sub.6 H.sub.5
5. 130
4-CH.sub.2 C.sub.6 H.sub.5
5. 131
2-CH.sub.2 C.sub.6 H.sub.5, 4-CH.sub.3
5. 132
2-CH.sub.3, 4-CH.sub.2 C.sub.6 H.sub.5
5. 133
2-C.sub.6 H.sub.5
5. 134
3-C.sub.6 H.sub.5
5. 135
4-C.sub.6 H.sub.5
5. 136
4-(2-i-C.sub.3 H.sub.7C.sub.6 H.sub.4)
5. 137
4-C.sub.6 H.sub.5, 2,6-(CH.sub.3).sub.2
5. 138
2-Cl, 4-C.sub.6 H.sub.5
5. 139
2-Br, 4-C.sub.6 H.sub.5
5. 140
2-C.sub.6 H.sub.5, 4-Cl
5. 141
2-C.sub.6 H.sub.5, 4-Br
5. 142
2-CH.sub.2 C.sub.6 H.sub.5, 4-Cl
5. 143
2-CH.sub.2 C.sub.6 H.sub.5, 4-Br
5. 144
2-Cl, 4-CH.sub.2 C.sub.6 H.sub.5
5. 145
2-Br, 4-CH.sub.2 C.sub.6 H.sub.5
5. 146
2-cyclo-C.sub.6 H.sub.11, 4-Cl
5. 147
2-cyclo-C.sub.6 H.sub.11, 4-Br
5. 148
2-Cl, 4-cyclo-C.sub.6 H.sub.11
5. 149
2-Br, 4-cyclo-C.sub.6 H.sub.11
5. 150
3-OCH.sub.3 oil 1742, 1670, 1597, 1276,
1011, 755
5. 151
2,4-(OCH.sub.3).sub.2
5. 152
2-CF.sub.3
5. 153
3-CF.sub. 3
5. 154
4-CF.sub.3
5. 155
2-OCF.sub.3
5. 156
3-OCF.sub.3
5. 157
4-OCF.sub.3
5. 158
OCH.sub.2 CHF.sub.2
5. 159
2-NO.sub.2
5. 160
3-NO.sub.2
5. 161
2-CN
5. 162
3-CN
5. 163
4-CN
5. 164
2-CH.sub.3, 3-Cl
5. 165
2-CH.sub.3, 5-Cl
5. 166
2-CH.sub.3, 6-Cl
5. 167
2-CH.sub.3, 3-F
5. 168
2-CH.sub.3, 4-F
5. 169
2-CH.sub.3, 5-F
5. 170
2-CH.sub.3, 6-F
5. 171
2-CH.sub.3, 3-Br
5. 172
2-CH.sub.3, 4-Br
5. 173
2-CH.sub.3, 5-Br
5. 174
2-CH.sub.3, 6-Br
5. 175
2-Cl, 3-CH.sub.3
5. 176
2-Cl, 4-CH.sub.3
5. 177
2-Cl, 5-CH.sub.3
5. 178
2-F, 3-CH.sub.3
5. 179
2-F, 4-CH.sub.3
5. 180
2-F, 5-CH.sub.3
5. 181
2-Br, 3-CH.sub.3
5. 182
2-Br, 4-CH.sub.3
5. 183
3-CH.sub.3, 4-Cl
5. 184
3-CH.sub.3, 5-Cl
5. 185
2-Br, 5-CH.sub.3
5. 186
3-CH.sub.3, 4-F
5. 187
3-CH.sub.3, 5-F
5. 188
3-CH.sub.3, 4-Br
5. 189
3-CH.sub.3, 5-Br
5. 190
3-F, 4-CH.sub.3
5. 191
3-Cl, 4-CH.sub.3
5. 192
3-Br, 4-CH.sub.3
5. 193
2-Cl, 4,5-(CH.sub.3).sub.2
5. 194
2-Br, 4,5-(CH.sub.3).sub.2
5. 195
2-Cl, 3,5-(CH.sub.3).sub.2
5. 196
2-Br, 3,5-(CH.sub.3).sub.2
5. 197
2,6-Cl.sub.2, 4-CH.sub.3
5. 198
2,6-F.sub.2, 4-CH.sub.3
5. 199
2,6-Br.sub.2, 4-CH.sub.3
5. 200
2,4-Cl.sub.2, 6-CH.sub.3
5. 201
2,4-F.sub.2, 6-CH.sub.3
5. 202
2,4-Br.sub.2, 6-CH.sub.3
5. 203
2,6-(CH.sub.3).sub.2, 4-F
5. 204
2,6-(CH.sub.3).sub.2, 4-Cl
5. 205
2,6-(CH.sub.3).sub.2, 4-Br
5. 206
3,5-(CH.sub.3).sub.2, 4-F
5. 207
3,5-(CH.sub.3).sub.2, 4-Cl
5. 208
3,5-(CH.sub.3).sub.2, 4-Br
5. 209
2,3,6-(CH.sub.3).sub.3, 4-F
5. 210
2,3,6-(CH.sub.3).sub.3, 4-Cl
5. 211
2,3,6-(CH.sub.3).sub.3, 4-Br
5. 212
2,4-(CH.sub.3).sub.2, 6-F
5. 213
2,4-(CH.sub.3).sub.2, 6-Cl
5. 214
2,4-(CH.sub.3).sub.2, 6-Br
5. 215
2-i-C.sub.3 H.sub.7, 4-Cl, 5-CH.sub.3
5. 216
2-Cl, 4-NO.sub.2
5. 217
2-NO.sub.2, 4-Cl
5. 218
2-OCH.sub.3, 5-NO.sub.2
5. 219
2,4-Cl.sub.2 , 5-NO.sub.2
5. 220
2,4-Cl.sub.2, 6-NO.sub.2
5. 221
2,6-Cl.sub.2, 4-NO.sub.2
5. 222
2,6-Br.sub.2, 4-NO.sub.2
5. 223
2,6-I.sub.2, 4-NO.sub.2
5. 224
2-CH.sub.3, 5-i-C.sub.3 H.sub.7, 4-Cl
5. 225
2-C.sub.6 H.sub.5 O
5. 226
3-C.sub.6 H.sub.5 O
5. 227
4-C.sub.6 H.sub.5 O
5. 228
3-t-C.sub.4 H.sub.9 O
5. 229
4-t-C.sub.4 H.sub.9 O
5. 230
*1)
5. 231
*2)
______________________________________
##STR19##
##STR20##
Claims (8)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3917352A DE3917352A1 (en) | 1989-05-27 | 1989-05-27 | NEW OXIMETERS AND FUNGICIDES CONTAINING THEM |
| DE3917352 | 1989-05-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US5145980A true US5145980A (en) | 1992-09-08 |
Family
ID=6381551
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/509,588 Expired - Fee Related US5145980A (en) | 1989-05-27 | 1990-04-16 | Oxime ethers, and fungicides containing same |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US5145980A (en) |
| EP (1) | EP0400417A1 (en) |
| JP (1) | JPH0317052A (en) |
| KR (1) | KR900018010A (en) |
| AU (1) | AU632124B2 (en) |
| CA (1) | CA2014781A1 (en) |
| DE (1) | DE3917352A1 (en) |
| HU (1) | HU206586B (en) |
| IL (1) | IL94083A (en) |
| NZ (1) | NZ233815A (en) |
| ZA (1) | ZA904024B (en) |
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| US5710314A (en) * | 1994-09-30 | 1998-01-20 | Novartis Corporation | Microbicides |
| US5763440A (en) * | 1994-11-14 | 1998-06-09 | Rohm And Haas Company | Pyridazinones and their use as fungicides |
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| US6080749A (en) * | 1994-12-16 | 2000-06-27 | Basf Aktiengesellschaft | Fungicidal mixture |
| US6211190B1 (en) | 1996-02-05 | 2001-04-03 | Basf Aktiengesellschaft | Pyrimidine derivatives, process and intermediate products for their preparation and pesticides or fungicides containing these derivatives |
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| DE3923093A1 (en) * | 1989-07-13 | 1991-01-24 | Basf Ag | NEW 3-METHOXIMINOPROPIONIC ACID ESTERS AND FUNGICIDES CONTAINING THEM |
| DE3932542A1 (en) * | 1989-09-29 | 1991-04-11 | Basf Ag | NEW ANILINE DERIVATIVES AND FUNGICIDES CONTAINING THEM |
| DE59108832D1 (en) * | 1990-12-31 | 1997-09-25 | Basf Ag | Process for the preparation of alpha-ketocarboxylic acid esters |
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- 1990-04-16 US US07/509,588 patent/US5145980A/en not_active Expired - Fee Related
- 1990-04-18 CA CA002014781A patent/CA2014781A1/en not_active Abandoned
- 1990-05-18 EP EP90109441A patent/EP0400417A1/en not_active Ceased
- 1990-05-24 AU AU55899/90A patent/AU632124B2/en not_active Ceased
- 1990-05-25 HU HU903206A patent/HU206586B/en not_active IP Right Cessation
- 1990-05-25 JP JP2134231A patent/JPH0317052A/en active Pending
- 1990-05-25 NZ NZ233815A patent/NZ233815A/en unknown
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|---|---|---|---|---|
| US5554619A (en) * | 1993-07-02 | 1996-09-10 | Ciba-Geigy Corporation | Microbicides |
| US5710314A (en) * | 1994-09-30 | 1998-01-20 | Novartis Corporation | Microbicides |
| US5763440A (en) * | 1994-11-14 | 1998-06-09 | Rohm And Haas Company | Pyridazinones and their use as fungicides |
| US5935961A (en) * | 1994-11-14 | 1999-08-10 | Rohm And Haas Company | Pyridazinones and their use as fungicides |
| US5958925A (en) * | 1994-11-14 | 1999-09-28 | Rohm And Haas Company | Pyridazinones and their use as fungicides |
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Also Published As
| Publication number | Publication date |
|---|---|
| EP0400417A1 (en) | 1990-12-05 |
| NZ233815A (en) | 1992-01-29 |
| JPH0317052A (en) | 1991-01-25 |
| AU5589990A (en) | 1990-09-27 |
| AU632124B2 (en) | 1992-12-17 |
| HU903206D0 (en) | 1990-10-28 |
| IL94083A (en) | 1995-03-30 |
| CA2014781A1 (en) | 1990-11-27 |
| DE3917352A1 (en) | 1990-11-29 |
| IL94083A0 (en) | 1991-01-31 |
| HUT54276A (en) | 1991-02-28 |
| ZA904024B (en) | 1992-01-29 |
| KR900018010A (en) | 1990-12-20 |
| HU206586B (en) | 1992-12-28 |
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